Methods of Making and Using Polyphenols Complexed With a Protein, Peptide, Amino Acid, Polysaccharide, Disaccharide, or Monosaccharide

ABSTRACT

The present invention a polyphenol complexes with amino acids, peptides, proteins, glycosaminoglycans, polysaccharides, mucopolysaccharide, disaccharides, monosaccharides, amino sugars, glycol-proteins, DNA/RNA oligonucleotides, mRNA, siRNA, antibodiesor other micro- or macro biomolecules.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Divisional Application of U.S. patent applicationSer. No. 15/819,305 filed Nov. 21, 2017, which claims priority based onU.S. Provisional Application Ser. No. 62/425,988, filed Nov. 23, 2016.The contents of each are incorporated by reference in their entirety.

TECHNICAL FIELD OF THE INVENTION

The present invention is in the field of formulations of nutraceuticals,and more specifically, to a polyphenol complexed with a protein,peptide, amino acid, polysaccharide, disaccharide, or monosaccharideused in nutraceuticals.

STATEMENT OF FEDERALLY FUNDED RESEARCH

None.

INCORPORATION-BY-REFERENCE OF MATERIALS FILED ON COMPACT DISC

None.

BACKGROUND OF THE INVENTION

Without limiting the scope of the invention, its background is describedin connection with polyphenol complexed with a protein, peptide, aminoacid, polysaccharide, disaccharide, or monosaccharide used innutraceuticals. Today there is a growing public awareness for healthynourishment that includes daily amounts of required micronutrients suchas vitamins, essential fatty acids and antioxidants. One source of thishealthy nourishment is nutraceuticals.

SUMMARY OF THE INVENTION

In the present invention a polyphenol (a turmeric extract or acurcuminoid, a grapeseed extract or a resveratrol, a milk thistleextract or silymarin or silibinin, or a green tea extract or EGCG orquercetin) complexes with proteins, peptides, amino acids,polysaccharides, disaccharides, monosaccharides, amino sugars,glycosaminoglycans, glycol-proteins. Also disclosed are methods ofpreparing a polyphenol complex, comprising obtaining a polyphenol (aturmeric extract or a curcuminoid, a grapeseed extract or a resveratrol,a milk thistle extract or silymarin or silibinin, or green tea extractor EGCG); obtaining a protein; and mixing the polyphenol and the proteinin a solvent. Also disclosed are methods of treating a subject, themethod comprising identifying a subject in need of treatment of apolyphenol-related disorder, and administering to the subject anutraceutical composition comprising a polyphenol-protein complex asdescribed. Also disclosed are methods of preparing a polyphenol complex,comprising obtaining a polyphenol; obtaining a peptide; and mixing thepolyphenol and the peptide in a solvent. Also disclosed are methods oftreating a subject, the method comprising identifying a subject in needof treatment of a polyphenol-related disorder, and administering to thesubject a nutraceutical composition comprising a polyphenol-peptidecomplex as described. Also disclosed are methods of preparing apolyphenol complex, comprising obtaining a polyphenol; obtaining anamino acid; and mixing the polyphenol and the amino acid in a solvent.Also disclosed are methods of treating a subject, the method comprisingidentifying a subject in need of treatment of a polyphenol-relateddisorder, and administering to the subject a nutraceutical compositioncomprising a polyphenol-acid complex as described. Also disclosed aremethods of preparing a polyphenol complex, comprising obtaining apolyphenol; obtaining a polysaccharide; and mixing the polyphenol andthe polysaccharide in a solvent. Also disclosed are methods of treatinga subject, the method comprising identifying a subject in need oftreatment of a polyphenol-related disorder, and administering to thesubject a nutraceutical composition comprising apolyphenol-polysaccharide complex as described. Also disclosed aremethods of preparing a polyphenol complex, comprising obtaining apolyphenol; obtaining a disaccharide; and mixing the polyphenol and thedisaccharide in a solvent. Also disclosed are methods of treating asubject, the method comprising identifying a subject in need oftreatment of a polyphenol-related disorder, and administering to thesubject a nutraceutical composition comprising a polyphenol-disaccharidecomplex as described. Also disclosed are methods of preparing apolyphenol complex, comprising obtaining a polyphenol; obtaining amonosaccharide; and mixing the polyphenol and the monosaccharide in asolvent. Also disclosed are methods of treating a subject, the methodcomprising identifying a subject in need of treatment of apolyphenol-related disorder, and administering to the subject anutraceutical composition comprising a polyphenol-monosaccharide complexas described. Also disclosed are nutraceutical compositions comprising apolyphenol complexed with a protein, peptide, amino acid,polysaccharide, disaccharide, or monosaccharide as described and apharmaceutically acceptable excipient, diluent, or carrier.

The present invention provided a polyphenol complex comprising atherapeutically effective amount of one or more polyphenols selectedfrom a turmeric extract, a curcumin, a curcuminoid, a grapeseed extract,a resveratrol, a milk thistle extract, a silymarin, a silibinin, a greentea extract, a epigallocatechin gallate and a quercetin; and one or morecomplexing agents conjugated to a therapeutically effective amount ofone or more polyphenols, wherein the one or more complexing agents areselected from proteins, peptides, amino acids, polysaccharides,disaccharides, monosaccharides, amino sugars, glycosaminoglycans, andglycol-proteins, disposed in a pharmaceutically acceptable excipient,diluent, or carrier.

The therapeutically effective amount of one or more polyphenols may benon-covalently conjugated to the complexing agent. The therapeuticallyeffective amount of one or more polyphenols may be 2, 3, 4, 5, 6, ormore polyphenols. The proteins may be selected from Whey proteinisolate, Egg protein isolate, Oat protein isolate, Hemp protein,Sunflower protein isolate Pea protein isolate, soybean protein isolate,fishmeal, flaxseed and Brown rice protein isolate. The one or morecomplexing agents may be N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan. The one or morecomplexing agents may be Cysteine, N-Acetyl cysteine, Methionine, DLmethionine, L methionine, Tyrosine, taurine. The one or more complexingagents may be Glutathione. The therapeutically effective amount of oneor more polyphenols comprise a turmeric extract and the one or morecomplexing agents are selected from whey protein isolate, egg proteinisolate, oat protein isolate, hemp protein, sunflower protein isolatepea protein isolate, soybean protein isolate, fishmeal, flaxseed, brownrice protein isolate, N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan, Cysteine, N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine, taurine,Glycose aminoglycans, mucopolysaccharides, polysaccharide, Chondroitinsulfate and Glucosamine sulfate, Glutathione, or a combination thereof.The therapeutically effective amount of one or more polyphenols comprisea curcuminoid and the one or more complexing agents are selected fromwhey protein isolate, egg protein isolate, oat protein isolate, hempprotein, sunflower protein isolate pea protein isolate, soybean proteinisolate, fishmeal, flaxseed, brown rice protein isolate,N-acetylglucosamine, glucosamine sulfate or N-acetylgalactosamine,glucuronic acid, iduronic acid, galactose chondroitin and glucosamine,glycosaminoglycan, Cysteine, N-Acetyl cysteine, Methionine, DLmethionine, L methionine, Tyrosine, taurine, Glycose aminoglycans,mucopolysaccharides, polysaccharide, Chondroitin sulfate and Glucosaminesulfate, Glutathione, or a combination thereof. The therapeuticallyeffective amount of one or more polyphenols comprise a resveratrol andthe one or more complexing agents are selected from whey proteinisolate, egg protein isolate, oat protein isolate, hemp protein,sunflower protein isolate pea protein isolate, soybean protein isolate,fishmeal, flaxseed, brown rice protein isolate, N-acetylglucosamine,glucosamine sulfate or N-acetylgalactosamine, glucuronic acid, iduronicacid, galactose chondroitin and glucosamine, glycosaminoglycan,Cysteine, N-Acetyl cysteine, Methionine, DL methionine, L methionine,Tyrosine, taurine, Glycose aminoglycans, mucopolysaccharides,polysaccharide, Chondroitin sulfate and Glucosamine sulfate,Glutathione, or a combination thereof. The therapeutically effectiveamount of one or more polyphenols comprise a silibinin and the one ormore complexing agents are selected from whey protein isolate, eggprotein isolate, oat protein isolate, hemp protein, sunflower proteinisolate pea protein isolate, soybean protein isolate, fishmeal,flaxseed, brown rice protein isolate, N-acetylglucosamine, glucosaminesulfate or N-acetylgalactosamine, glucuronic acid, iduronic acid,galactose chondroitin and glucosamine, glycosaminoglycan, Cysteine,N-Acetyl cysteine, Methionine, DL methionine, L methionine, Tyrosine,taurine, Glycose aminoglycans, mucopolysaccharides, polysaccharide,Chondroitin sulfate and Glucosamine sulfate, Glutathione, or acombination thereof. The therapeutically effective amount of one or morepolyphenols comprise Epigallocatechin gallate and the one or morecomplexing agents are selected from whey protein isolate, egg proteinisolate, oat protein isolate, hemp protein, sunflower protein isolatepea protein isolate, soybean protein isolate, fishmeal, flaxseed, brownrice protein isolate, N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan, Cysteine, N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine, taurine,Glycose aminoglycans, mucopolysaccharides, polysaccharide, Chondroitinsulfate and Glucosamine sulfate, Glutathione, or a combination thereof.The therapeutically effective amount of one or more polyphenols comprisequercetin and the one or more complexing agents are selected from wheyprotein isolate, egg protein isolate, oat protein isolate, hemp protein,sunflower protein isolate pea protein isolate, soybean protein isolate,fishmeal, flaxseed, brown rice protein isolate, N-acetylglucosamine,glucosamine sulfate or N-acetylgalactosamine, glucuronic acid, iduronicacid, galactose chondroitin and glucosamine, glycosaminoglycan,Cysteine, N-Acetyl cysteine, Methionine, DL methionine, L methionine,Tyrosine, taurine, Glycose aminoglycans, mucopolysaccharides,polysaccharide, Chondroitin sulfate and Glucosamine sulfate,Glutathione, or a combination thereof. The therapeutically effectiveamount of one or more polyphenols comprise a milk thistle extract andthe one or more complexing agents are selected from whey proteinisolate, egg protein isolate, oat protein isolate, hemp protein,sunflower protein isolate pea protein isolate, soybean protein isolate,fishmeal, flaxseed, brown rice protein isolate, N-acetylglucosamine,glucosamine sulfate or N-acetylgalactosamine, glucuronic acid, iduronicacid, galactose chondroitin and glucosamine, glycosaminoglycan,Cysteine, N-Acetyl cysteine, Methionine, DL methionine, L methionine,Tyrosine, taurine, Glycose aminoglycans, mucopolysaccharides,polysaccharide, Chondroitin sulfate and Glucosamine sulfate,Glutathione, or a combination thereof.

The present invention provides a nutraceutical composition comprising atherapeutically effective amount of one or more polyphenols selectedfrom a turmeric extract, a curcumin, a curcuminoid, a grapeseed extract,a resveratrol, a milk thistle extract, a silymarin, a silibinin, a greentea extract, a epigallocatechin gallate and a quercetin; and one or morecomplexing agents conjugated to a therapeutically effective amount ofone or more polyphenols, wherein the one or more complexing agents areselected from proteins, peptides, amino acids, polysaccharides,disaccharides, monosaccharides, amino sugars, glycosaminoglycans,glycol-proteins disposed in a pharmaceutically acceptable excipient,diluent, or carrier.

The present invention provides a method of treating a subject sufferingfrom a polyphenol-related disorder comprising the steps of: identifyinga subject in need of treatment of a polyphenol-related disorder; andadministering to the subject a nutraceutical composition comprising apolyphenol-acid complex comprising a therapeutically effective amount ofone or more polyphenols selected from a turmeric extract, a curcumin, acurcuminoid, a grapeseed extract, a resveratrol, a milk thistle extract,a silymarin, a silibinin, a green tea extract, a epigallocatechingallate and a quercetin; and one or more complexing agents conjugated toa therapeutically effective amount of one or more polyphenols, whereinthe one or more complexing agents are selected from proteins, peptides,amino acids, polysaccharides, disaccharides, monosaccharides, aminosugars, glycosaminoglycans, glycol-proteins disposed in apharmaceutically acceptable excipient, diluent, or carrier.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the features and advantages of thepresent invention, reference is now made to the detailed description ofthe invention along with the accompanying figures and in which:

DETAILED DESCRIPTION OF THE INVENTION

While the making and using of various embodiments of the presentinvention are discussed in detail below, it should be appreciated thatthe present invention provides many applicable inventive concepts thatcan be embodied in a wide variety of specific contexts. The specificembodiments discussed herein are merely illustrative of specific ways tomake and use the invention and do not delimit the scope of theinvention.

To facilitate the understanding of this invention, a number of terms aredefined below. Terms defined herein have meanings as commonly understoodby a person of ordinary skill in the areas relevant to the presentinvention. Terms such as “a”, “an” and “the” are not intended to referto only a singular entity, but include the general class of which aspecific example may be used for illustration. The terminology herein isused to describe specific embodiments of the invention, but their usagedoes not delimit the invention, except as outlined in the claims.

As used herein the term “Conjugation” follows any Conjugationmethodology known to the skilled artisan but generally includes thepolyphenol being solubilized with a solvent (ethanol, methanol, etc.)under heat ˜50° C., pressure, proper pH (depending on polyphenol) andprotected from light while mixing/solubilizing and the mixture is cooledto warmed temperatures (37-45° C.). The conjugate material (proteins,polysaccharides, etc.) is added and allowed to mix for a period of time.A vacuum is created to lower boiling point and vaporizing the solventfor removal and drying of the material. In some instances, it ispossible to combine two polyphenols with a conjugate material, e.g.,Curcumin and resveratrol can be mixed and conjugated withpolysaccharide, or glucosamine sulfate or chondroitin sulfate or apeptide or an amino acid or a protein; or in another embodiment,curcumin and milk thistle (silymarin and/or silibinin) can be mixed andconjugated with polysaccharide, or glucosamine sulfate or chondroitinsulfate or a peptide or an amino acid or a protein; or in anotherembodiment, curcumin and green tea (EGCG) can be mixed and conjugatedwith polysaccharide, or glucosamine sulfate or chondroitin sulfate or apeptide or an amino acid or a protein; or in another embodiment,curcumin and quercetin can be mixed and conjugated with polysaccharide,or glucosamine sulfate or chondroitin sulfate or a peptide or an aminoacid or a protein. In some instances, it is possible to combine morethan two polyphenols a with conjugate material, e.g., Curcumin,resveratrol and milk thistle (silymarin and/or silibinin) can be mixedand conjugated with a polysaccharide, or glucosamine sulfate orchondroitin sulfate or a peptide or an amino acid or a protein; or inanother embodiment, curcumin, green tea (EGCG) and milk thistle(silymarin and/or silibinin) can be mixed and conjugated with apolysaccharide, or glucosamine sulfate or chondroitin sulfate or apeptide or an amino acid or a protein; or in another embodiment,curcumin, resveratrol, green tea (EGCG) and milk thistle (silymarinand/or silibinin) can be mixed and conjugated with a polysaccharide, orglucosamine sulfate or chondroitin sulfate or a peptide or an amino acidor a protein;

As used herein the term “Flavonols” denotes derivatives of flavonoidsthat use the 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-oneskeleton. Quercetin (a polyphenol flavonoid) can be conjugated toproteins, peptides & amino acids including proteins like Whey proteinisolate, Egg protein isolate, Oat protein isolate, Hemp protein,Sunflower protein isolate and Brown rice protein isolate; Peptides likeGlutathione; Amino acids like Cysteine or Methionine; Conjugatedpolysaccharides like Glycose aminoglycans (GAG)—mucopolysaccharides,Polysaccharides, Chondroitin sulfate and Glucosamine sulfate.

As used herein the term “Flavonolignans” denotes derivatives of naturalphenols composed of a part flavonoid and a part lignan. Milk Thistle(Silybum marianum) with active constituents including Sylimarin andsilibinin can be conjugated to proteins, peptides & amino acidsincluding proteins like Whey protein isolate, Egg protein isolate, Oatprotein isolate, Hemp protein, Sunflower protein isolate and Brown riceprotein isolate; Peptides like Glutathione; Amino acids like Cysteine orMethionine; Conjugated polysaccharides like Glycose aminoglycans(GAG)—mucopolysaccharides, Polysaccharide, Chondroitin sulfate andGlucosamine sulfate.

As used herein the term “Curcuminoids” (other polyphenols) denotesderivatives of Turmeric (Curcuma longa). A phytopolyphenol pigmentisolated from the plant Curcuma longa, commonly known as turmeric, witha variety of pharmacologic properties. Curcumin blocks the formation ofreactive-oxygen species, possesses anti-inflammatory properties as aresult of inhibition of cyclooxygenases (COX) and other enzymes involvedin inflammation; and disrupts cell signal transduction by variousmechanisms including inhibition of protein kinase C. These effects mayplay a role in the agent's observed antineoplastic properties, whichinclude inhibition of tumor cell proliferation and suppression ofchemically induced carcinogenesis and tumor growth in animal models ofcancer. Curcuminoids (including curcumin, bisdemethoxycurcumin,demethoxycurcumin) can be conjugated to proteins, peptides & amino acidsincluding proteins like Whey protein isolate, Egg protein isolate, Oatprotein isolate, Hemp protein, Sunflower protein isolate and Brown riceprotein isolate; Peptides like Glutathione; Amino acids like Cysteine orMethionine; Conjugated polysaccharides like Glycose aminoglycans(GAG)—mucopolysaccharides, Polysaccharides, Chondroitin sulfate andGlucosamine sulfate.

As used herein the term “polyphenol” denotes a structural class ofmainly natural, but also synthetic or semisynthetic, organic chemicalscharacterized by the presence of multiples of phenol structural units.The number and characteristics of these phenol structures underlie theunique physical, chemical, and biological properties (e.g., metabolic,toxic, therapeutic, etc.). Examples include (but not limited to)curcumin (curcuminoids), quercetin, resveratrol, Silymarin, silibinin,tannic acid, Epigallocatechin gallate (EGCG), and ellagitannin. Thegeneral physical properties include water-insoluble, moderatelywater-insoluble and moderately water-soluble compounds with molecularweight of 500-4000 Da, >12 phenolic hydroxyl groups, and 5-7 aromaticrings per 1000 Da (these are general ranges and may be ±20% and bewithin the definition of polyphenol. Examples of polyphenol include butare not limited to and include derivatives thereof: trans-Resveratrol,Curcumin, Quercetin, Silymarin (standardized Milk Thistle extract), andEpigallocatechin gallate (EGCG—standardized Green Tea extract).

As used herein the term “proteins” denotes large biomolecules, ormacromolecules, consisting of one or more long chains of amino acidresidues and includes natural and synthetic and modified R groups toachieve natural, synthetic or modified amino acids. Proteins includeWhey protein isolate, Egg protein isolate, Oat protein isolate, Hempprotein, Sunflower protein isolate and Brown rice protein isolate, Otherproteins (variable conjugations), Pea protein isolate, soybean proteinisolate, fishmeal & flaxseed. Amino acids include Cysteine & N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine (noconjugation), taurine and the like. N-Acetyl-L-cysteine is the N-acetylderivative of cysteine. It is used as a mucolytic agent to reduce theviscosity of mucous secretions. It has also been shown to have antiviraleffects in patients with HIV due to inhibition of viral stimulation byreactive oxygen intermediates. Methionine is one of nine essential aminoacids in humans (provided by food), Methionine is required for growthand tissue repair. A sulphur-containing amino acid, methionine improvesthe tone and pliability of skin, hair, and strengthens nails. Involvedin many detoxifying processes, sulphur provided by methionine protectscells from pollutants, slows cell aging, and is essential for absorptionand bio-availability of selenium and zinc. Methionine chelates heavymetals, such as lead and mercury, aiding their excretion. It also actsas a lipotropic agent and prevents excess fat buildup in the liver.

As used herein the term “peptides” denotes small biomolecules, ormacromolecules, consisting of one or more short chains of amino acidresidues. The term “peptide” in the context of a “peptide compound” or a“peptide complex” is meant as a compound having at least two amino acidslinked together by a peptide bond. In some embodiments, the peptide isan oligopeptide, for example a bipeptide, having two amino acids, atripeptide, having three amino acids, a 4-mer, 5-mer, and the like. Insome embodiments, the peptide is an oligopeptide comprises between 2-20amino acids. In other embodiments, the peptide is a polypeptide havingbetween 21-100 amino acids. Glutathione is a tripeptide comprised ofthree amino acids (cysteine, glutamic acid, and glycine) present in mostmammalian tissue. Glutathione acts as an antioxidant, a free radicalscavenger and a detoxifying agent. Glutathione is also important as acofactor for the enzyme glutathione peroxidase, in the uptake of aminoacids, and in the synthesis of leukotrienes. As a substrate forglutathione S-transferase, this agent reacts with a number of harmfulchemical species, such as halides, epoxides and free radicals, to formharmless inactive products. In erythrocytes, these reactions preventoxidative damage through the reduction of methemoglobin and peroxides.Glutathione is also involved in the formation and maintenance ofdisulfide bonds in proteins and in the transport of amino acids acrosscell membranes.

As used herein the term “carrier” denotes a chemical compound thatfacilitates the incorporation of a compound into cells or tissues. Forexample, dimethyl sulfoxide (DMSO) is a commonly utilized carrier as itfacilitates the uptake of many organic compounds into the cells ortissues of an organism. A common carrier is water, where an aqueoussolution of the product of interest is prepared and administered to asubject.

As used herein the term “diluent” denotes chemical compounds diluted inwater that will dissolve the compound of interest as well as stabilizethe biologically active form of the compound. Salts dissolved inbuffered solutions are utilized as diluents in the art. One commonlyused buffered solution is phosphate buffered saline because it mimicsthe salt conditions of human blood. Since buffer salts can control thepH of a solution at low concentrations, a buffered diluent rarelymodifies the biological activity of a compound.

In certain embodiments, the same substance can act as a carrier,diluent, or excipient, or have any of the two roles, or have all threeroles. Thus, a single additive to the pharmaceutical composition canhave multiple functions.

As used herein the term “physiologically acceptable” denotes a carrieror diluent that does not abrogate the biological activity and propertiesof the compound.

As used herein the term “Stilbenes” denotes an organic compound with theformula (C₆H₅CH)₂. Classified as a diarylethene, it features a centralethene double bond substituted with phenyl groups on each carbon atomsof the double bond. Examples include Resveratrol (Trans-resveratrol(98%) and Resveratrol (50% standardized grape seed extract). Resveratrolis a phytoalexin derived from grapes and other food products withantioxidant and potential chemopreventive activities. Resveratrolinduces phase II drug-metabolizing enzymes (anti-initiation activity);mediates anti-inflammatory effects and inhibits cyclooxygenase andhydroperoxidase functions (anti-promotion activity); and inducespromyelocytic leukemia cell differentiation (anti-progression activity),thereby exhibiting activities in three major steps of carcinogenesis.This agent may inhibit TNF-induced activation of NF-kappaB in a dose-and time-dependent manner. Resveratrol and trans-resveratrol can beconjugated to proteins, peptides & amino acids including proteins likeWhey protein isolate, Egg protein isolate, Oat protein isolate, Hempprotein, Sunflower protein isolate and Brown rice protein isolate;Peptides like Glutathione; Amino acids like Cysteine or Methionine;Conjugated polysaccharides like Glycose aminoglycans(GAG)-mucopolysaccharides, Polysaccharides, Chondroitin sulfate andGlucosamine sulfate.

As used herein the term “subject” denotes an animal, preferably amammal, and most preferably a human, who is the object of treatment,observation or experiment. The mammal may be selected from the groupconsisting of mice, rats, rabbits, guinea pigs, dogs, cats, sheep,goats, pigs, cows, horses, primates, such as monkeys, chimpanzees, andapes, and humans. Other animals include wildlife (deer, elk, moose,bear, lion, rhinoceros, elephant, etc.), avian (birds, poultry, chicken,turkey, duck, etc.), reptiles (snake, turtle, tortoise, lizard, etc.)and fish (freshwater, saltwater, etc.).

As used herein the term “therapeutically effective amount” denotes anamount of the polyphenol complexed with a protein, peptide, amino acid,polysaccharide, disaccharide or monosaccharide that elicits thebiological or medicinal response indicated. This response may occur in atissue, system, animal or human that is being sought by a researcher,veterinarian, medical doctor or other clinician, and includesalleviation of the symptoms of the disease being treated.

As used herein the term “treat,” “treating,” “treatment,” or any othervariation thereof, does not indicate the complete cure from a disorder.Any amelioration of alleviation of the symptoms of a diseases ordisorder to any degree, or any increase in the comfort of the subject,is considered treatment.

As used herein the term “Glycosaminoglycans” denotes (GAGs) ormucopolysaccharides are long unbranched polysaccharides consisting of arepeating disaccharide unit. The repeating unit consists of an aminosugar (N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine) along with an uronic sugar (glucuronic acid oriduronic acid) or galactose. For example, chondroitin and glucosamine.Chondroitin sulfate is a sulfated glycosaminoglycan (GAG) composed of achain of alternating sugars (N-acetylgalactosamine and glucuronic acid).It is usually found attached to proteins as part of a proteoglycan. Achondroitin chain can have over 100 individual sugars, each of which canbe sulfated in variable positions and quantities. Chondroitin sulfate isan important structural component of cartilage and provides much of itsresistance to compression. Glucosamine is commonly used as a treatmentfor osteoarthritis. It is an amino sugar and a prominent precursor inthe biochemical synthesis of glycosylated proteins and lipids. Sinceglucosamine is a precursor for glycosaminoglycans, andglycosaminoglycans are a major component of joint cartilage,supplemental glucosamine may help to rebuild cartilage and treatarthritis. Other polysaccharides include fucoidan (sulfatedpolysaccharide) obtained from brown algae and brown seaweed.

As used herein the term “Resveratrol” denotes(3,5,4′-trihydroxy-trans-stilbene or pterostilbene) a stilbenoid, a typeof natural phenol, and a phytoalexin produced naturally by severalplants in response to injury or when the plant is under attack bypathogens such as bacteria or fungi. Resveratrol is thought to achievecardioprotective effects by a number of different routes: (1) Inhibitionof vascular cell adhesion molecule expression; (2) Inhibition ofvascular smooth muscle cell proliferation; (3) Stimulation ofendolethelial nitric oxide synthase (eNOS) activity; (4) Inhibition ofplatelet aggregation; and (5) Inhibition of LDL peroxidation. Althoughtrans-Resveratrol is shown below cis-Resveratrol is also consideredherein.

As used herein the term “EGCG” denotes Epigallocatechin gallate, alsoknown as epigallocatechin-3-gallate, is the ester of epigallocatechinand gallic acid, and is a type of catechin. Epigallocatechin Gallate isa phenolic antioxidant found in a number of plants such as green andblack tea. It inhibits cellular oxidation and prevents free radicaldamage to cells. EGCG, the most abundant catechin in tea, is apolyphenol.

As used herein the term “Quercetin” denotes a flavonoid widelydistributed in nature and is the aglycone form of a number of otherflavonoid glycosides, such as rutin and quercetin, found in citrusfruit, buckwheat and onions. Quercetin is a polyphenolic flavonoid withpotential chemopreventive activity. Quercetin, ubiquitous in plant foodsources and a major bioflavonoid in the human diet, may produceantiproliferative effects resulting from the modulation of either EGFRor estrogen-receptor mediated signal transduction pathways. Although themechanism of action is not fully known, the following effects have beendescribed with this agent in vitro: decreased expression of mutant p53protein and p21-ras oncogene, induction of cell cycle arrest at the G1phase and inhibition of heat shock protein synthesis. This compound alsodemonstrates synergy and reversal of the multidrug resistance phenotype,when combined with chemotherapeutic drugs, in vitro. Quercetin alsoproduces anti-inflammatory and anti-allergy effects mediated through theinhibition of the lipoxygenase and cyclooxygenase pathways, therebypreventing the production of pro-inflammatory mediators.

As used herein the term “Silymarin” also known as Milk Thistle, denotesa standardized extract of the milk thistle seeds, containing a mixtureof flavonolignans consisting of silymarin, silibinin, isosilibinin,silicristin, silidianin, and others. Silibinin is the major activeconstituent of silymarin, a standardized extract of the milk thistleseeds, containing a mixture of flavonolignans consisting of silibinin,isosilibinin, silicristin, silidianin and others. Silibinin itself ismixture of two diastereomers, silybin A and silybin B, in approximatelyequimolar ratio. Both in vitro and animal research suggest thatsilibinin has hepatoprotective (antihepatotoxic) properties that protectliver cells against toxins. Silibinin has also demonstrated in vitroanti-cancer effects against human prostate adenocarcinoma cells,estrogen-dependent and -independent human breast carcinoma cells, humanectocervical carcinoma cells, human colon cancer cells, and both smalland nonsmall human lung carcinoma cells.

As used herein the term “curcuminoid” denotes a linear diarylheptanoid,with molecules such as curcumin or derivatives of curcumin withdifferent chemical groups that have been formed to increase solubilityof curcumins and make them suitable for drug formulation. Thesecompounds are natural phenols and produce a pronounced yellow color.Turmeric extracts or curcuminoids include Curcumin (95% curcuminoids),Curcumin, Desmethoxycurcumin, Bisdesmethoxycurcumin, Tetrahydrocurcumin,Tetrahydrodesmethoxycurcumin, Tetrahydrobisdesmethoxycurcumin andderivatives thereof.

The present inventors have discovered that the ingestion of apolyphenol-protein complex, or polyphenol-peptide complex orpolyphenol-amino acid complex or polyphenol-polysaccharide complex orpolyphenol-disaccharide or polyphenol-monosaccharide complexsignificantly increases solubility and the serum bioavailability of thepolyphenol as compared to the ingestion of uncomplexed polyphenol.

Thus, in one aspect, disclosed herein are polyphenol-protein complex, orpolyphenol-peptide complex or polyphenol-amino acid complex orpolyphenol-polysaccharide complex or polyphenol-disaccharide orpolyphenol-monosaccharide complex comprising a polyphenol compoundlinked to a protein compound or peptide compound or an amino acid or apolysaccharide compound or a disaccharide compound or a monosaccharide.In other embodiments, the peptide compound is a protein or a proteinfragment. In some embodiments, a protein is naturally occurring and is afull sequence polypeptide expressed by a cell. In other embodiments, aprotein is a synthetic protein having a sequence that is not found innature. In some embodiments, the synthetic protein is expressed by acell using recombinant technologies, whereas in other embodiments, thesynthetic protein is synthesized using a peptide synthesizer. A proteinfragment is an oligo- or polypeptide having a sequence identical to asequence fragment found in a protein.

In some embodiments, the polyphenol compound is linked covalently to aprotein compound or peptide compound or an amino acid or apolysaccharide compound or a disaccharide compound or a monosaccharide.In these embodiments, the polyphenol compound is either bound directlyto an amino acid of the peptide, or is bound through a linker compound.In some embodiments, the linker is an alkyl, alkenyl, or alkenyl moiety,which may be substituted with a substituent selected from the groupconsisting of —OH, —SH, —SO, —COOH, —N—C(O)H, —N—C(O)OH, —C(O)NH, andthe like. In some embodiment, the linker is bound to the amino acid orthe polyphenol compound through a substituent. In other embodiments, thepolyphenol compound is linked by hydrogen bonding to the peptidecompound to form the complex. In yet other embodiments, the polyphenolcompound is linked by electrostatic forces to the protein compound (orpeptide compound or an amino acid or a polysaccharide compound or adisaccharide compound or a monosaccharide) to form the complex. In yetother embodiments, the polyphenol compound is linked by lipophilicinteractions (e.g., van der Waals forces) to the protein compound (orpeptide compound or an amino acid or a polysaccharide compound or adisaccharide compound or a monosaccharide) to form the complex. In someembodiments, the peptide is a full-length protein. In certainembodiments, the protein is one that is found in the serum of a mammal.In other embodiments, the protein is derived from an animal source otherthan a mammal. In still other embodiment, the protein is derived fromplants, such as grains, legumes, fruits, vegetables, and the like.

Examples of oligo- and polypeptides and full-length proteins used in thecomplexes described herein include, but are not limited to whey protein,tumor necrosis factor (TNF-α); cyclooxygenase (COX) (including COX-1 andCOX-2); al-acid glycoprotein (AGP) (also known as orosomucoid); myeloiddifferentiation protein 2 (MD-2); any one of the group of enzymes calledhistone acetyl-transferases (HATs), such as p300/CBP; any one of thegroup of enzymes called histone deacetylases (HDAC); glyoxalase I(GLOI); xanthine oxidase (XO); a proteasome; sarco (endo) plasmicreticulum Ca²⁺ ATPase (SERCA); human immunodeficiency virus type 1(HIV-1) protease; any one of the DNA methyltransferases (DNMTs), forexample DNMT1; DNA polymerase (pol) any one of the ribonucleases(RNases), for example RNase A; any one of the lipoxygenases (LOXs); anyone of the matrix metalloproteinases (MMPs); lysozyme; any one of theprotein kinase C (PKC) family of enzymes; cellular sarcoma (c-Src);glycogen synthase kinase (GSK)-3β; ErbB2; phosphorylase kinase; any oneof the protein reductases, for example thioredoxin reductase (TrxR) andaldose reductase (ALR2); thioredoxin reductase; any one of the caseins;human serum albumin (HSA); bovine serum albumin (BSA); fibrinogen;β-lactoglobulin (β-LG); α-lactalbumin; human serum immunoglobulin (Ig);FtsZ; transthyretin (TTR); glutathione (GSH); and Kelch-likeECH-associated protein 1 (Keap1).

In some embodiments, the polyphenol-protein complex is a complex ofpolyphenol and whey protein isolate or a brown rice protein isolate. Incertain embodiments the polyphenol is a curcuminoid (turmeric extract),or a milk thistle extract (e.g., silymarin and/or silibinin), or aresveratrol, or a green tea extract (e.g., EGCG) or quercetin. Incertain embodiments, the whey protein is a milk-derived whey protein orthe brown rice protein is a plant derived protein. Milk whey protein isa mixture of 0-lactoglobulin (˜65%), α-lactalbumin (˜25%), bovine serumalbumin (˜8%), and immunoglobulins. In some of these embodiments, thecomplex is formed by mixing the polyphenol and the whey protein isolatein ethanol. Thus, in these embodiments, there is no covalent linkagebetween the polyphenol and the whey protein. In certain embodiments, theratio of polyphenol to whey protein or brown rice protein is 1:20 w/w.In other embodiments the ratio of a non-curcuminoid polyphenol to wheyprotein or brown rice protein is 1:≥40 and 1:≤50 w/w or polyphenol towhey protein or brown rice protein in any increment between 1:>10 and1:<40. In other embodiments the ratio of non-curcuminoid polyphenol towhey protein or brown rice protein is 1:50 w/w. In some embodiments, thewhey protein is obtained from a commercially available source, whichcomprises 85-90% whey protein in the available powder. In someembodiments, the brown rice protein is obtained from a commerciallyavailable source, which comprises 80-90% brown rice protein in theavailable powder. In some embodiments, the polyphenol is a curcuminoid,or a milk thistle extract (e.g., silymarin and/or silibinin), or aresveratrol, or a green tea extract (e.g., EGCG) or quercetin and isobtained from a commercially available source.

In some embodiments, the polyphenol-protein complex is a complex ofpolyphenol and sunflower protein or oat protein. In certain embodimentsthe polyphenol is a curcuminoid (turmeric extract), or a milk thistleextract (e.g., silymarin and/or silibinin), or a resveratrol, or a greentea extract (e.g., EGCG) or quercetin. In certain embodiments, thesunflower protein is a plant derived protein or the oat protein is aplant derived protein. In some of these embodiments, the complex isformed by mixing the polyphenol and the sunflower protein or the oatprotein in ethanol. Thus, in these embodiments, there is no covalentlinkage between the polyphenol and the sunflower protein or the oatprotein. In certain embodiments, the ratio of polyphenol to sunflowerprotein or oat protein is 1:20 w/w. In other embodiments the ratio ofpolyphenol to sunflower protein or oat protein is 1:≥40 and 1:≤50 w/w orpolyphenol to sunflower protein or oat protein in any increment between1:>20 and 1:<40. In some embodiments, the sunflower protein is obtainedfrom a commercially available source, which comprises 60-70% sunflowerprotein in the available powder. In some embodiments, the oat protein isobtained from a commercially available source, which comprises 60-70%oat protein in the available powder. In some embodiments, the polyphenolis a curcuminoid, or a milk thistle extract (e.g., silymarin and/orsilibinin), or a resveratrol, or a green tea extract (e.g., EGCG) orquercetin and is obtained from a commercially available source.

In some embodiments, the polyphenol-protein complex is a complex ofpolyphenol and hemp protein or flaxseed protein. In certain embodimentsthe polyphenol is a curcuminoid (turmeric extract), or a milk thistleextract (e.g., silymarin and/or silibinin), or a resveratrol, or a greentea extract (e.g., EGCG) or quercetin. In certain embodiments, the hempprotein is a plant derived protein or the flaxseed protein is a plantderived protein. In some of these embodiments, the complex is formed bymixing the polyphenol and the hemp protein or the flaxseed protein inethanol. Thus, in these embodiments, there is no covalent linkagebetween the polyphenol and the hemp protein (isolate) or the flaxseedprotein (isolate). In certain embodiments, the ratio of polyphenol tohemp protein or flaxseed protein is 1:<100 w/w. In other embodiments theratio of a polyphenol to hemp protein or flaxseed protein is 1:≥50 and1:≤100 w/w or polyphenol to hemp protein or flaxseed protein in anyincrement between 1:>40 and 1:<50. In some embodiments, the hemp proteinis obtained from a commercially available source, which comprises 60-70%hemp protein in the available powder. In some embodiments, the flaxseedprotein is obtained from a commercially available source, whichcomprises 60-70% flaxseed protein in the available powder. In someembodiments, the polyphenol is a curcuminoid, or a milk thistle extract(e.g., silymarin and/or silibinin), or a resveratrol, or a green teaextract (e.g., EGCG) or quercetin and is obtained from a commerciallyavailable source.

In another aspect, disclosed herein is a nutraceutical compositioncomprising a polyphenol-peptide complex, as described herein, and apharmaceutically acceptable carrier, diluent, or excipient. In certainembodiments the polyphenol is a curcuminoid (turmeric extract), or amilk thistle extract (e.g., silymarin and/or silibinin), or aresveratrol, or a green tea extract (e.g., EGCG) or quercetin. Incertain embodiments the peptide is a tripeptide. In other embodimentsthe peptide is glutathione. In some embodiments the glutathione whichcomprises the three amino acids L-cysteine, L-glutamic acid and glycineis obtained from a commercially available source. The sulfhydryl groupof cysteine is primarily responsible for the biological activity ofglutathione. As an important antioxidant, glutathione can decreaseintra-cellular damage caused by ROS (reactive oxidative species). Insome of these embodiments, the complex is formed by mixing thepolyphenol and the glutathione in ethanol. Thus, in these embodiments,there is no covalent linkage between the polyphenol and the glutathione.In certain embodiments, the ratio of polyphenol to glutathione is 1:<10w/w. In other embodiments the ratio of a polyphenol glutathione is 1:≥10and 1:≤20 w/w or polyphenol to glutathione in any increment between 1:≥1and 1:≤20.

In another aspect, disclosed herein is a nutraceutical compositioncomprising a polyphenol-amino acid complex, as described herein, and apharmaceutically acceptable carrier, diluent, or excipient. In certainembodiments the polyphenol is a curcuminoid (turmeric extract), or amilk thistle extract (e.g., silymarin and/or silibinin), or aresveratrol, or a green tea extract (e.g., EGCG) or quercetin. Incertain embodiments the amino acid is cysteine. In other embodiments thecysteine amino acid is N-Acetyl-cysteine and is available from acommercially available source. N-acetyl cysteine is a white crystallinepowder with a slight odor and sour taste. N-acetyl-cysteine is solublein water and ethanol. N-acetyl-cysteine molecular formula is C₅H₉NO₃Sand a molecular weight of 163.191 g/mol. The sulfhydryl group ofcysteine is primarily responsible for the biological activity ofN-acetyl-cysteine. In some embodiments the amino acid is methionine. Inother embodiments the methionine is DL-methionine orN-acetyl-DL-methionine or L-methionine or D-methionine and is availablefrom a commercially available source. The molecular formula forDL-methionine is C₄H₁₁NO₂S and the molecular weight is 149.208 g/mol.Methionine is an essential amino acid required for growth and tissuerepair. In some of these embodiments, the complex is formed by mixingthe polyphenol and the amino acid, n-acetyl-cysteine or DL-methionine,in ethanol. Thus, in these embodiments, there is no covalent linkagebetween the polyphenol and the amino acid n-acetyl-cysteine orDL-methionine. In certain embodiments, the ratio of polyphenol toN-acetyl-cysteine or DL-methionine is 1:1, 1:2, 1:4 or 1:≤10 w/w. Inother embodiments the ratio of a polyphenol to N-acetyl-cysteine orDL-methionine is 1:≥10 and 1:≤20 w/w or polyphenol to N-acetyl-cysteineor DL-methionine in any increment between 1:≥1 and 1:≤20.

In other embodiments, disclosed herein include a nutraceuticalcomposition comprising a polyphenol-disaccharide complex, as describedherein, and a pharmaceutically acceptable carrier, diluent, orexcipient. In certain embodiments the polyphenol is a curcuminoid(turmeric extract), or a milk thistle extract (e.g., silymarin and/orsilibinin), or a resveratrol, or a green tea extract (e.g., EGCG) orquercetin. In certain embodiments the disaccharide is chondroitin. Inother embodiments chondroitin is chondroitin sulfate and is an animal orplant derived mucopolysaccharide or glycosaminoglycan and is availablefrom a commercially available source. Chondroitin sulfate is a whitepowder and soluble in water and ethanol. Chondroitin sulfate molecularformula is C₁₃H₂₁NO₁₅S and a molecular weight of 463.363 g/mol. In someof these embodiments, the complex is formed by mixing the polyphenol andthe chondroitin sulfate in ethanol. Thus, in these embodiments, there isno covalent linkage between the polyphenol and chondroitin sulfate. Incertain embodiments, the ratio of polyphenol to chondroitin sulfate is1:1, 1:2, 1:4 or 1:≤10 w/w. In other embodiments the ratio of apolyphenol to chondroitin sulfate is 1:≥10 and 1:≤20 w/w or the ratio ofa polyphenol to chondroitin sulfate in any increment between 1:≥1 and1:≤20.

In other embodiments, disclosed herein include a nutraceuticalcomposition comprising a polyphenol-monosaccharide complex, as describedherein, and a pharmaceutically acceptable carrier, diluent, orexcipient. In certain embodiments the polyphenol is a curcuminoid(turmeric extract), or a milk thistle extract (e.g., silymarin and/orsilibinin), or a resveratrol, or a green tea extract (e.g., EGCG) orquercetin. In certain embodiments the monosaccharide is glucosamine. Inother embodiments glucosamine is glucosamine sulfate and is an animal orplant derived monosaccharide and is available from a commerciallyavailable source. glucosamine sulfate is a white powder and soluble inwater and ethanol. glucosamine sulfate molecular formula is C₁₃H₂₁NO₁₅Sand a molecular weight of 463.363 g/mol. In some of these embodiments,the complex is formed by mixing the polyphenol and the glucosaminesulfate in ethanol. Thus, in these embodiments, there is no covalentlinkage between the polyphenol and glucosamine sulfate. In certainembodiments, the ratio of polyphenol to glucosamine sulfate is 1:1, 1:2,1:4 or 1:≤10 w/w. In other embodiments the ratio of a polyphenol toglucosamine sulfate is 1:≥10 and 1:≤20 w/w or the ration of a polyphenolto glucosamine sulfate in any increment between 1:≥1 and 1:≤20.

In another aspect, disclosed herein is a nutraceutical compositioncomprising a polyphenol complexed with a protein, peptide, amino acid,polysaccharide, disaccharide or monosaccharide, as described herein, anda pharmaceutically acceptable carrier, diluent, or excipient. Thenutraceutical compositions disclosed herein may be manufactured in amanner that is itself known, e.g., by means of conventional mixing,dissolving, granulating, dragee-making, levigating, emulsifying,encapsulating, entrapping or tableting processes. Nutraceuticalcompositions disclosed herein thus may be formulated in conventionalmanner using one or more physiologically acceptable carriers comprisingexcipients and auxiliaries which facilitate processing of thepolyphenol-peptide complexed with a protein, peptide, amino acid,polysaccharide, disaccharide or monosaccharide into preparations whichcan be used nutraceutically or as a food ingredient (e.g., drink mixes,chocolate, gummies, granola, soup mixes, etc.). Any of the well-knowntechniques, carriers, and excipients may be used as suitable and asunderstood in the art; e.g., in Remington's Pharmaceutical Sciences,above.

For oral administration, the polyphenol complexed with a protein,peptide, amino acid, polysaccharide, disaccharide or monosaccharide canbe formulated readily by combining the polyphenol complexed with aprotein, peptide, amino acid, polysaccharide, disaccharide ormonosaccharide with pharmaceutically acceptable carriers well known inthe art. Such carriers enable the presently disclosed complexes to beformulated as tablets, pills, dragees, capsules, liquids, gels, syrups,slurries, suspensions and the like, for oral ingestion by a subject.Nutraceutical preparations for oral use can be obtained by mixing one ormore solid excipient with the disclosed polyphenol-peptide complexes,optionally grinding the resulting mixture, and processing the mixture ofgranules, after adding suitable auxiliaries, if desired, to obtaintablets or dragee cores. Suitable excipients are, in particular, fillerssuch as sugars, including lactose, sucrose, mannitol, or sorbitol;cellulose preparations such as, for example, maize starch, wheat starch,rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose,hydroxypropylmethyl-cellulose, sodium carboxymethylcellulose, and/orpolyvinylpyrrolidone (PVP). If desired, disintegrating agents may beadded, such as the cross-linked polyvinylpyrrolidone, agar, or alginicacid or a salt thereof such as sodium alginate.

Dragee cores are provided with suitable coatings. For this purpose,concentrated sugar solutions may be used, which may optionally containgum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethyleneglycol, and/or titanium dioxide, lacquer solutions, and suitable organicsolvents or solvent mixtures. Dyestuffs or pigments may be added to thetablets or dragee coatings for identification or to characterizedifferent combinations of active compound doses.

Nutraceutical preparations that can be used orally include push-fitcapsules made of gelatin, as well as soft, sealed capsules made ofgelatin and a plasticizer, such as glycerol or sorbitol. The push-fitcapsules can contain the active ingredients in admixture with fillersuch as lactose, binders such as starches, and/or lubricants such astalc or magnesium stearate and, optionally, stabilizers. In softcapsules, the active compounds may be dissolved or suspended in suitableliquids, such as fatty oils, liquid paraffin, or liquid polyethyleneglycols. In addition, stabilizers may be added. All formulations fororal administration should be in dosages suitable for suchadministration.

Nutraceutical compositions suitable for use in the methods disclosedherein include compositions where the polyphenol-peptide complex iscontained in an amount effective to achieve its intended purpose. Morespecifically, a therapeutically effective amount means an amount of thepolyphenol-peptide complex effective to prevent, alleviate or amelioratesymptoms of disease or prolong the survival of the subject beingtreated.

Typically, the dose range of the polyphenol-complexed with a protein,peptide, amino acid, polysaccharide, disaccharide or monosaccharideadministered to the patient is from about 0.5 to 100 mg/kg of thepatient's body weight. The dosage may be a single one or a series of twoor more given in the course of one or more days, as is needed by thepatient. In some embodiments, the dosage is between 0.1 mg to 50 mg. Inother embodiments, the dosage is between 1 mg to 10 mg. Other doseranges include between 10 to 50 mg, between 20 to 50 mg, between 30 to50 mg, between 40 to 50 mg, between 20 to 40 mg, between 10 to 20 mg,between 10 to 30 mg, between 20 to 30 mg, and between 30 to 40 mg. Thedose may also be at 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80mg, 90 mg, 100 mg, 110 mg, 120 mg, 130 mg, 140 mg, 150 mg, 160 mg, 170mg, 180 mg, 190 mg, or 200 mg. As used above the dosage refers to activeagent dosage and cam be in up to 100 mg or 150 mg. In some embodiments,the dosage is 600 mg s.i.d. (once a day). In another embodiment, thepolyphenol-complexed with a protein, peptide amino acid, polysaccharide,disaccharide or monosaccharide when given orally, the total dosage is600-1200 mg per os b.i.d (twice a day) or 600-1200 mg per os t.i.d.(three times a day) or 600-1200 mg per os or 600-1200 mg per os q.i.d.(four times a day)

In another aspect, disclosed herein is a method of treating a disorder,the method comprising identifying a subject in need thereof andadministering to the subject a therapeutically effect amount of apolyphenol complex as disclosed herein.

In another aspect, disclosed herein is a method of treating a disorder,the method comprising identifying a subject in need thereof andadministering to the subject a therapeutically effect amount of apolyphenol complexed with a protein, peptide, amino acid,polysaccharide, disaccharide or monosaccharide as disclosed herein,where subsequent to the administration, the serum Cmax of polyphenolis >1 ng/ml<2,000 ng/mL. In some embodiments, the serum Cmax ofpolyphenol is <0.001% of the administered dose of polyphenol. Thedefinition of the pharmacokinetic parameter C_(max) is well-known tothose of skill in the art. Briefly, C_(max) is the maximum observedplasma concentration after a dosage administration.

In another aspect, disclosed herein is a method of preparing apolyphenol complexed with a protein, peptide, amino acid,polysaccharide, disaccharide or monosaccharide, as described above, themethod comprising obtaining a polyphenol; obtaining a protein; obtaininga peptide; obtaining an amino acid; obtaining a polysaccharide;obtaining a disaccharide; or obtaining a monosaccharide and mixing thepolyphenol and the protein or the peptide or the amino acid or thepolysaccharide or the disaccharide or the monosaccharide in a solvent.In some embodiments, the solvent is a polar solvent, while in otherembodiments, the solvent is an apolar solvent. In some embodiments, thepolar solvent is water, whereas in other embodiments, the polar solventis an alcohol. In some embodiments, the alcohol is ethanol or methanol

Example 1: Preparation of polyphenol-Whey Protein Complex. Apolyphenol-whey protein complex was prepared for administration to humansubjects. The following materials were used: Whey Protein was 90%protein by weight, polyphenol was 95% by weight and 100% ethyl alcohol.Ratio of polyphenol:whey protein of 1:20 w/w. A 0.5% w/v tincture(solution) was prepared by mixing 50 g curcumin powder with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes or until solution turned clear. To the resulting solution wasadded 950 g whey protein isolate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a fine and orange colored powder. Thepowder re-solubilizes in water with stirring. Alternative method—In avacuum blender the polyphenol is added to a 2000 ml. solvent (methanol,acetate, ethanol) at the rate of 25 grams per liter. The mixture isblended at 50° C. for 60 minutes or until mixture is clear. 475 grams ofwhey protein per liter solvent is added and continued mixing at 40° C.for thirty minutes. Low vacuum is applied to remove solvent until dry.Ratio of a single polyphenol:whey protein of 50 mg polyphenol: 1 gmpowder or 1:20 w/w. The above procedure was repeated, except with 25 gpolyphenol powder and 1000 g brown rice protein isolate powder. Asimilar product was obtained with a ration of 1:20 w/w of polyphenol tobrown rice protein. The above procedure was repeated, except with 25 gpolyphenol powder and 1000 g brown rice protein isolate powder. Asimilar product was obtained with a ration of 1:20 w/w of polyphenol tobrown rice protein. The above procedure was repeated, except with gcurcumin powder (95%) and 1000 g brown rice protein isolate powder. Asimilar product was obtained with a ration of 1:20 w/w of polyphenol tobrown rice protein

Example 2: Administration of polyphenol-Whey protein Complex. Twohealthy individuals were administered a single dose of thepolyphenol-whey complex, having a ratio of polyphenol:whey of 25 mg: 1gm w/w. The dosage contained 25 mg of polyphenol. Blood was drawn fromeach individual at 20 min, 50 min, and 90 min, and the level of serumpolyphenol was calculated.

Curcumin-chondroitin, Curcumin-glucosamine, Curcumin-polysaccharide,Resveratrol-peptide, Resveratrol-amino acid, Resveratrol-chondroitin,Resveratrol-glucosamine, Resveratrol-polysaccharide, EGCG-peptide,EGCG-amino acid, EGCG-chondroitin, EGCG-glucosamine,EGCG-polysaccharide, Quercetin-peptide, Quercetin-amino acid,Quercetin-chondroitin, Quercetin-glucosamine, Quercetin-polysaccharide,Silymarin-peptide, Silymarin-amino acid, Silymarin-chondroitin,Silymarin-polysaccharide and Silymarin-glucosamine.

The present invention includes a composition having Curcuminoid-proteinconjugates. In this embodiment the protein may be a natural or syntheticprotein and may be of any length, e.g., dipeptide, tripeptides,polypeptides, oligopeptides, etc. The peptide may be conjugated toCurcuminoid, where the peptide is an amino acid. The compositions may bemade by solvent assisted blending of curcuminoid-protein conjugates,curcuminoid-peptide conjugates and curcuminoid-amino acid conjugates.

The formulations may include the active agent in communication with apolysaccharide, mucopolysaccharide, glycosaminoglycan, disaccharide,monosaccharide or a amino sugar that is synthetic or naturallyoccurring. For example, the composition may be curcuminoid-glucosamineconjugates, and Curcuminoid-chondroitin conjugates.

The formulations may include the non-curcuminoid polyphenols,resveratrol Conjugates, resveratrol-proteins, resveratrol-peptides,resveratrol-amino acid, resveratrol-polysaccharide,resveratrol-glucosamine, and resveratrol-chondroitin. The process ofmaking these conjugates include solvent assisted blending ofresveratrol-protein conjugates, resveratrol-peptide conjugates andresveratrol-amino acid conjugates and examples of the formulationincludes 10-250 mg resveratrol per 1 gram peptides, amino acids and/orsaccharides. In other instances formulations include 10-50 mgresveratrol per 1 gram protein. These formulations may be used in animalformulations and human formulations.

The formulations may include the non-curcuminoid polyphenols,Epigallocatechin gallate (EGCG-Green Tea extracts) conjugates likeEGCG-protein, EGCG-peptides, EGCG-amino acid, EGCG-polysaccharide,EGCG-glucosamine and EGCG-chondroitin. The process of making theseconjugates include solvent assisted blending. Examples of theformulation includes 10-100 mg EGCG per 1 gram peptides, or 1 gramn-acetyl-cysteine or 1 gram DL-methionine or 1 gram chondroitin sulfateor 1 gram glucosamine sulfate. In other instances, formulations include10-50 mg EGCG per 1 gram protein. Theses formulations may be used inanimal formulations and human formulations as antioxidant,anti-inflammatory, immune stimulant, etc.

The formulations may include the non-curcuminoid polyphenols, likequercetin conjugates and examples of the formulation includequercetin-protein, Quercetin-peptides, quercetin-amino acid,quercetin-polysaccharide, quercetin-glucosamine orquercetin-chondroitin. The process of making these conjugates includesolvent assisted blending of conjugates and examples of the formulationincludes 10-250 mg quercetin per 1 gram peptides, or 1 gramn-acetyl-cysteine or 1 gram DL-methionine or 1 gram chondroitin sulfateor 1 gram glucosamine sulfate. In other instances, formulations include10-50 mg EGCG per 1 gram protein. These formulations may be used inanimal formulations and human formulations.

The formulations may include the non-curcuminoid polyphenols, likeSilymarin (silibinin) Milk Thistle extract conjugates and examples ofthe formulation include Silymarin-proteins, Silymarin-peptides,Silymarin-amino acid, Silymarin-polysaccharide, Silymarin-glucosamineand Silymarin-chondroitin. The process of making these conjugatesinclude solvent assisted blending of curcuminoid-conjugates. Thesesformulations may be used in animal formulations including humanformulations. Examples of the formulation includes 10-250 mg Silymarinper 1 gram peptides, or 1 gram n-acetyl-cysteine or 1 gram DL-methionineor 1 gram chondroitin sulfate or 1 gram glucosamine sulfate. In otherinstances, formulations include 10-50 mg Silymarin per 1 gram protein.These formulations may be used in animal formulations and humanformulations.

In any of the embodiments may include common peptides (proteins) to beused including Proteins like whey, brown rice, egg, hemp protein,flaxseed protein, etc.; Amino acids—cysteine, methionine; saccharides tobe used include glucosamine, polysaccharide & chondroitin.

The formulations may include curcumin-chondroitin conjugates, usingchondroitin sulfate-mucopolysaccharide (sulfated glycosaminoglycan)which is a white crystalline powder and 247.30 g/mol, chemical formulaC₁₄H₁₉O₁₄S, with a melting point about 190-194° C., is water solublehaving a pH 5.5-7.5 and may come from marine or animal sources.Chondroitin sulfate is produced from enzymatic digestion of bovinepoultry, porcine and marine animal cartilaginous tissues. The benefitsinclude as a dietary supplement for joint health since chondroitinsulfate is a major component of cartilage. Loss of chondroitin sulfatefrom the cartilage is a major cause of osteoarthritis.Methodology/Preparation. curcumin solubility in water is very poor.Organic solvents (methanol, acetone, DMSO, etc.) will increasesolubility. An example of the curcumin-chondroitin sulfate complex isprepared using the following materials: Chondroitin sulfate about 99%;Curcumin powder about 95% curcuminoids (Turmeric longa) by weight;Silica (or diatomaceous earth) about 100%; Ethanol about 95% ethylalcohol. The composition is processed by blending/Processing: 50 gramscurcumin with 1-liter ethanol is placed in a rotary mixing vessel atroom temperature and medium speed (20 rpm) and blended for 2 hours; 500grams chondroitin sulfate powder and 25 grams silica are added withcontinued mixing for another 30 minutes; and a low vacuum is generatedin the vessel to remove the ethanol solvent. The resulting powder is afine, slightly crystalline, off-white color and able to solubilize inwater. The ratio of curcumin:chondroitin sulfate is 1:10 w/w.

The formulations include curcumin-Glucosamine conjugate usingglucosamine sulfate, which is a white crystalline powder with a 277.2496g/mol and a chemical formula C₆H₁₅NO₉S and a melting point about 192° C.The source may be from Marine (shellfish, crustacean)—primary andfermentation of grains (primarily corn or wheat). It is slightly watersoluble. The benefits include as a dietary supplement for joint health.The methodology/preparation of the curcumin-glucosamine sulfate complexis prepared using the following materials: glucosamine sulfate about99%; curcumin powder about 95% curcuminoids (Turmeric longa) by weight;silica (or diatomaceous earth) about 100%; ethanol about 95% ethylalcohol. The processing is done by blending/processing: 50 gramscurcumin with 1-liter ethanol is placed in a rotary mixing vessel atroom temperature and medium speed (20 rpm) and blended for 2 hours. 500grams of glucosamine sulfate powder and 25 grams silica are added withcontinued mixing for another 30 minutes. A low vacuum is generated inthe vessel to remove the ethanol solvent. Resulting powder is a fine,slightly crystalline, off-white color and able to solubilize in water.The ratio of curcumin:glucosamine sulfate is 1:10 w/w.

The formulations include resveratrol formulation conjugates of peptides,proteins, Amino acids, Polysaccharides, mucopolysaccharides,saccharides, chondroitin, glucosamine, Naturally occurring polyphenol,Stilbene class, stilbenoids, trans-resveratrol(3,5,4′-trihydroxy-trans-stilbene), Active form, with a mol. wt. about228.25, chem. Formula C₁₄H₁₂O₃. Other names includetrans-3,5,4′-Trihydroxystilbene, Pterostilbene, 3,4′,5-Stilbenetriol,trans-Resveratrol, cis-resveratrol, (E)-5-(p-Hydroxystyryl) resorcinol,(E)-5-(4-hydroxystyryl) benzene-1,3-diol, Pterostilbene with a mol.wt.-256.296 and a chem. formula C₁₆H₁₆O₃ Synonym(3,5-Dimethyl-resveratrol). Resveratrol has a mol. wt. about 228.243,chem. formula C₁₄H₁₂O₃ synonym (3,5,4′-Trihydroxystilbene). Resveratrol3-O-glucoside has a mol. wt. about 390.384 and a chem. formula C₂₀H₂₂O₈synonym (Piceid Polydatin). Resveratrol 5-O-glucoside has a mol. wt. of390.384 with a chem. formula—C₂₀H₂₂O₈.

Resveratrol is a stilbene polyphenolic compounds, has cis and trans twoconfiguration, wherein the trans is the stable structure, and thebiological activity is broader. It was first discovered that the grapescontained these substances in 1970s, and through years of research anddiscovery, it was found that resveratrol not just present in grapes, butpresent in many fruits, plants and nuts. In 1992, resveratrol was firstdiscovered in commercial wine. Studies shows that resveratrol (transresveratrol) help to protect the body immune system, lower cholesterol,lower blood pressure, boost energy, helps skin look younger and helpsburn fat. Other benefits include anti-oxidant, anti-inflammatory effectson acute and chronic inflammation, support cardio vascular system,protect and stimulate the immune system, protect againstneurodegenerative diseases, cancer prevention, and weight loss. Sourcesinclude grapes (skin), extracts of the root of Polygonum cuspidatum,Japanese knotweed, peanuts, cocoa, berries, blueberries, bilberries, andcranberries.

Resveratrol peptide conjugates include dipeptides, tripeptides,polypeptides, oligopeptides, proteins, protein fragments, etc. Examplesof protein and peptide sources include animal, plant and synthetic. Themethods of preparation includes organic solvents (methanol, acetone,DMSO, etc.) to increase solubility from 0.03 to 16-50 grams/Liter. Anexample of the resveratrol-whey protein complex is prepared using wheyprotein about 85-90% protein by weight, resveratrol powder about 98%resveratrol (Polygonum cuspidatum) by weight, ethanol about 95% ethylalcohol. The blending process includes adding 50 grams resveratrolpowder with about 1 liter ethanol is placed in a rotary mixing vessel atroom temperature and slow speed (15 rpm) and blended for 1 hour, 1kilogram whey protein is added with continued mixing for another 30minutes. A low vacuum is generated in the vessel to remove the ethanolsolvent and the resulting powder is a fine off-white color and able tosolubilize in water. The ratio of resveratrol:whey protein is 1:20 w/w.

Resveratrol-amino acid conjugates include cysteine, methionine, etc.Cysteine is a white crystalline powder with a MW of 121.15 g/mol and thechemical formula C₃H₇NO₂S and a melting point about 240° C. It isavailable from plant and animal. It is also water soluble and slightlyinsoluble in ethanol. An example of the resveratrol-cysteine complex isprepared using the following materials: L-cysteine powder about 99%,Resveratrol powder about 98% resveratrol (Polygonum cuspidatum) byweight, Silica (or diatomaceous earth) about 100%, ethanol about 95%ethyl alcohol. The processing or blending includes adding 50 gramsresveratrol with 1-liter ethanol is placed in a rotary mixing vessel atroom temperature and medium speed (20 rpm) and blended for 2 hours. 500grams cysteine powder and 25 grams silica are added with continuedmixing for another 30 minutes. A low vacuum is generated in the vesselto remove the ethanol solvent. The resulting powder is a fine, slightlycrystalline, off-white color and able to solubilize in water. The ratioof resveratrol:cysteine is approximately 1:10 w/w.

Resveratrol-chondroitin conjugates use chondroitin sulfate (sulfatedglycosaminoglycan) mucopolysaccharide which is a white crystallinepowder with a MW of 247.30 g/mol and a chemical formula C₁₄H₁₉O₁₄S,melting point of 190-194° C., and is available from animals and marine.It is water soluble and has a ph 5.5-7.5. Chondroitin sulfate isproduced from enzymatic digestion of bovine, poultry, porcine and marineanimal cartilaginous tissues. The benefits include joint health sincechondroitin sulfate is a major component of cartilage. loss ofchondroitin sulfate from the cartilage is a major cause ofosteoarthritis. Resveratrol has very poor (0.03 grams/liter) solubilityin water so organic solvents (methanol, acetone, dmso, etc.) are used toincrease solubility (16-50 grams/liter). The resveratrol-chondroitinsulfate complex is prepared using chondroitin sulfate about 99%,resveratrol powder about 98% resveratrol (Polygonum cuspidatum) byweight, silica (or diatomaceous earth) about 100%, and ethanol about 95%ethyl alcohol. The processing or blending includes combining 50 gramsresveratrol with 1-liter ethanol is placed in a rotary mixing vessel atroom temperature and medium speed (20 rpm) and blended for 2 hours and500 grams chondroitin sulfate powder and 25 grams silica are added withcontinued mixing for another 30 minutes. A low vacuum is generated inthe vessel to remove the ethanol solvent and the resulting powder is afine, slightly crystalline, off-white color and able to solubilize inwater. The ratio of resveratrol:chondroitin sulfate is 1:10 w/w.

The present invention provides resveratrol-glucosamine conjugates usingglucosamine sulfate which is a white crystalline powder with a MW of277.2496 g/mol and a chemical formula C₆H₁₅NO₉S and a melting point of192° C. Glucosamine can be found in marine (shellfish, crustacean) andfermentation of grains (primarily corn or wheat). It is slightly watersoluble and provides benefits like joint health. An example of theresveratrol-glucosamine sulfate complex is prepared using the followingmaterials glucosamine sulfate about 99%, resveratrol powder about 98%resveratrol (Polygonum cuspidatum) by weight, silica (or diatomaceousearth) about 100%, ethanol about 95% ethyl alcohol. The processing orblending includes combining 50 grams resveratrol with 1 liter ethanol isplaced in a rotary mixing vessel at room temperature and medium speed(20 rpm) and blended for 2 hours and 500 grams glucosamine sulfatepowder and 25 grams silica are added with continued mixing for another30 minutes. A low vacuum is generated in the vessel to remove theethanol solvent resulting powder is a fine, slightly crystalline,off-white color and able to solubilize in water. The ratio ofresveratrol:glucosamine sulfate is 1:10 w/w.

The present invention provides Green tea extracts-EGCG(epi-gallocatechin gallate) conjugates. EGCG is a naturally occurringpolyphenol in the catechin family of flavonoids. The primary antioxidantingredients include green tea catechins (GTC), Epicatechin (EC),Epigallocatechin (EGC), Epicatechin gallate (ECG), and Epigallocatechin(EGCG)—accounts for more than 40% of the total content. EGCG has amolecular weight of 458.372 g/mol. and the chem. formula C₂₂H₁₈O₁₁ witha melting point of 218° C. EGCG has a water solubility of 5 mg/ml and anethanol solubility of 20 mg/ml. EGCG is a bitter, rust (brown-orange)fine powder. Sources include green tea, white tea, black tea, etc. andthe benefits include anti-oxidant, anti-inflammatory, inhibitsdevelopment of some cancers, and inhibits development of diabetes.Examples of EGCG-peptides conjugates include dipeptides, tripeptides,polypeptides, oligopeptides, proteins, protein fragments, etc. fromanimal, plant and synthetic sources. An example of the resveratrol-wheyprotein complex is prepared using the following materials: whey proteinabout 85-90% protein by weight, EGCG powder about 50%, and ethanol about95% ethyl alcohol. The processing or blending includes combining 25grams EGCG powder with 1 liter ethanol is placed in a rotary mixingvessel at room temperature and slow speed (15 rpm) and blended for 1hour and 500 grams whey protein is added with continued mixing foranother 30 minutes. A low vacuum is generated in the vessel to removethe ethanol solvent and the resulting powder is a fine off-white colorand able to solubilize in water and the ratio of EGCG:whey protein is1:20 w/w.

EGCG-amino acids conjugates include cysteine, methionine, etc. Forexample, the cysteine conjugates are available from plants and animalsand are a white crystalline powder with a MW of 121.15 g/mol, meltingpoint of about 240° C. and chemical formula C₃H₇NO₂S. It is solubilityin water and slightly insoluble in ethanol. An example of theEGCG-cysteine complex is prepared using L-cysteine powder about 99%,EGCG powder about 50%, Silica (or diatomaceous earth) about 100%, water(or organic solvent e.g., ethanol 95%). The processing or blendingincludes combining 50 grams EGCG with 1 liter water is placed in arotary mixing vessel at room temperature and medium speed (20 rpm) andblended for 2 hours and 500 grams cysteine powder and 25 grams silicaare added with continued mixing for another 30 minutes. A low vacuumunder mild heating (40° C.) is generated in the vessel to remove thewater and results in a fine powder, slightly crystalline, off-whitecolor and able to solubilize in water. The ratio of EGCG:cysteine isapproximately 1:10 w/w.

EGCG-chondroitin conjugates are prepared using chondroitin sulfate about99%, EGCG about 50% by weight, Silica (or diatomaceous earth) about100%, and Ethanol about 95% ethyl alcohol. The processing or blendingincludes combining 50 grams EGCG with 1 liter ethanol is placed in arotary mixing vessel at room temperature and medium speed (20 rpm) andblended for 2 hours and 500 grams chondroitin sulfate powder and 25grams silica are added with continued mixing for another 30 minutes. Alow vacuum is generated in the vessel to remove the ethanol solvent andresults in a fine powder, slightly crystalline, off-white color and ableto solubilize in water. The ratio of EGCG:chondroitin sulfate is 1:10w/w.

EGCG-glucosamine conjugates are prepared using glucosamine sulfate about99%, EGCG-50% by weight, silica (or diatomaceous earth) about 100%, andethanol about 95% ethyl alcohol. The processing or blending includescombining 50 grams EGCG with 1 liter ethanol is placed in a rotarymixing vessel at room temperature and medium speed (20 rpm) and blendedfor 2 hours and 500 grams glucosamine sulfate powder and 25 grams silicaare added with continued mixing for another 30 minutes. A low vacuum isgenerated in the vessel to remove the ethanol solvent and results in afine powder, slightly crystalline, off-white color and able tosolubilize in water. The ratio of EGCG:glucosamine sulfate is 1:10 w/w.

The present invention provides milk thistle-silymarin (silibinin)conjugates. Silymarin (silibinin) is a naturally occurring polyphenol.Milk thistle (Silybum marianum) has many complex structural componentsfrom the Flavonolignan (lignin family) group of polyphenols, e.g.,silymarin and silibinin-standardized extract from the seeds of milkthistle has three structural constituents, with silibinin being the mostactive, silydianin. Silychristin is water insoluble and soluble inorganic solvents (e.g., methanol, ethanol, DMSO) having a chem. formulaC₂₅H₂₂O₁₀ with a Mol. Wt. of 482.44 g/mol and is a light brown (tan)powder. The benefits include antioxidant, anti-inflammatory, inhibitsdevelopment of some cancers, and/or inhibits hepatotoxicity.

Silymarin (silibinin)-peptide conjugates include dipeptides,tripeptides, polypeptides, oligopeptides, proteins, protein fragments,etc. An example of the silymarin-whey protein complex is prepared usingwhey protein about 85-90% protein by weight, silymarin (silibinin) about80% (30%) and ethanol about 95% ethyl alcohol. The processing orblending includes combining 25 grams silymarin powder with 1 literethanol is placed in a rotary mixing vessel at room temperature and slowspeed (15 rpm) and blended for 1 hour and 500 grams whey protein isadded with continued mixing for another 30 minutes. A low vacuum isgenerated in the vessel to remove the ethanol solvent resulting in afine light tan color powder and able to solubilize in water. The ratioof silymarin:whey protein is 1:20 w/w.

Silymarin (silibinin)-amino acid conjugates include cysteine,methionine, etc. Silymarin-cysteine complex is prepared using 1-cysteinepowder about 99%, silymarin (silibinin) about 80% (30%) by wt., silica(or diatomaceous earth) about 100%, and water (or organic solvent—ex.ethanol 95%). The processing or blending includes combining 50 gramssilymarin with 1 liter ethanol is placed in a rotary mixing vessel atroom temperature and medium speed (20 rpm) and blended for 2 hours and500 grams N-acetyl-cysteine powder and 100 grams silica are added withcontinued mixing for another 30 minutes. A low vacuum under mild heating(40° C.) is generated in the vessel to remove the water, results in apowder that is a fine, slightly crystalline, light tan color and able tosolubilize in water. The ratio of silymarin:cysteine is approximately1:10 w/w.

Silymarin-chondroitin sulfate complex is prepared using chondroitinsulfate about 99%, silymarin (silibinin) about 80% (30%) by wt., silica(or diatomaceous earth) about 100%, and ethanol about 95% ethyl alcohol.The processing or blending includes combining 50 grams silymarin with 1liter ethanol is placed in a rotary mixing vessel at room temperatureand medium speed (20 rpm) and blended for 2 hours and 500 gramschondroitin sulfate powder and 50 grams silica are added with continuedmixing for another 30 minutes. A low vacuum is generated in the vesselto remove the ethanol solvent, resulting powder that is a fine, slightlycrystalline, off-white color and able to solubilize in water. The ratioof silymarin:chondroitin sulfate is 1:10 w/w.

An example of the silymarin-glucosamine sulfate complex is preparedusing glucosamine sulfate about 99%, silymarin (silibinin) about 80%(30%) by wt., silica (or diatomaceous earth) about 100% and ethanolabout 95% ethyl alcohol. The processing or blending includes combining50 grams silymarin with 1 liter ethanol is placed in a rotary mixingvessel at room temperature and medium speed (20 rpm) and blended for 2hours and 500 grams glucosamine sulfate powder and 50 grams silica areadded with continued mixing for another 30 minutes. A low vacuum isgenerated in the vessel to remove the ethanol solvent, resulting in apowder that is a fine, slightly crystalline, off-white color and able tosolubilize in water. The ratio of silymarin:glucosamine sulfate is 1:10w/w.

In another instance, more than one polyphenol may be complexed with aprotein, peptide, amino acid, polysaccharide, disaccharide, ormonosaccharide using the same methods described above. In someembodiments, the first polyphenol is a curcuminoid and the secondpolyphenol is a milk thistle extract (80% silymarin, 30% silibinin). Theprotein is whey protein isolate. Example 1—Preparation of curcumin/milkthistle extract-whey protein isolate complex. A curcumin/milk thistleextract-whey protein isolate complex was prepared for administration tohuman and animal subjects. The following materials were used: wheyprotein isolate was 90% protein by weight, curcumin was 95% curcuminoidsby weight, milk thistle extract was 80% silymarin (and 30% silibinin) byweight and 100% ethyl alcohol. Ratio of curcumin:milk thistleextract:whey protein isolate is 0.5:0.5:20 w/w. A 0.5% w/v tincture(solution) was prepared by mixing 25 g curcumin powder and 25 gram milkthistle extract powder with 2000 mL ethanol. The mixture was placed on amagnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes or until solution turnedclear. To the resulting solution was added 950 g whey protein isolatepowder. The mixture was placed on a rotary evaporator (rotovap) at slowspeed (20-30 rpm), having a water bath temperature of 50° C., and lowvacuum for 3-4 hours or until the ethanol was evaporated. Alternatively,the mixture was placed in a lyophilizer. The final product was a fineand yellow colored powder. The powder re-solubilizes in water withstirring. Alternative method—In a vacuum blender the curcumin and milkthistle extract are added to a 2000 ml. solvent (ethanol) at the rate of12.5 grams (each) per liter. The mixture is blended at 50° C. for 60minutes or until mixture is clear. 475 grams of whey protein per litersolvent is added and continued mixing at 40° C. for thirty minutes.Vacuum is applied to reactor to remove solvent until dry.

In some embodiments, the first polyphenol is a curcuminoid and thesecond polyphenol is a milk thistle extract (80% silymarin, 30%silibinin). The monosaccharide is glucosamine sulfate. Example 2−Preparation of curcumin/milk thistle extract-glucosamine sulfatecomplex. A curcumin/milk thistle extract-glucosamine sulfate complex wasprepared for administration to human and animal subjects. The followingmaterials were used: glucosamine sulfate was 99% by weight, curcumin was95% curcuminoids by weight, milk thistle extract was 80% silymarin (and30% silibinin) by weight and 100% ethyl alcohol. Ratio of curcumin:milkthistle extract:glucosamine sulfate is 1:1:4 w/w. A 0.5% w/v tincture(solution) was prepared by mixing 200 g curcumin powder and 200 grammilk thistle extract powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g glucosamine sulfate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and milk thistleextract are added to a 2000 ml. solvent (ethanol) at the rate of 100grams (each) per liter. The mixture is blended at 50° C. for 60 minutes.400 grams of glucosamine sulfate per liter solvent is added andcontinued mixing at 40° C. for thirty minutes. Vacuum is applied toreactor to remove solvent until dry. In another embodiment, using themethodology described above the ratio of curcumin to milk thistleextract to glucosamine sulfate is 1:1:2.

Example 3—Preparation of curcumin/milk thistleextract/resveratrol-glucosamine sulfate complex. A curcumin/milk thistleextract/resveratrol-glucosamine sulfate complex was prepared foradministration to human and animal subjects. The following materialswere used: glucosamine sulfate was 99% glucosamine sulfate by weight,curcumin was 95% curcuminoids by weight, milk thistle extract was 80%silymarin (and 30% silibinin) by weight, resveratrol as 98% by weightand 100% ethyl alcohol. Ratio of curcumin:milk thistleextract:resveratrol:glucosamine sulfate is 2:2:1:10 w/w. A 0.5% w/vtincture (solution) was prepared by mixing 200 g curcumin powder and 200gram milk thistle extract powder and 100 grams resveratrol with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes. To the resulting solution was added 1000 g glucosamine sulfatepowder. The mixture was placed on a rotary evaporator (rotovap) at slowspeed (20-30 rpm), having a water bath temperature of 50° C., and lowvacuum for 3-4 hours or until the ethanol was evaporated. Alternatively,the mixture was placed in a lyophilizer. The final product was acrystalline, fine and orange colored powder. The powder re-solubilizesin water with stirring. Alternative method—In a vacuum blender thecurcumin and milk thistle extract are added to a 2000 ml. solvent(ethanol) at the rate of 100 grams of curcumin, 100 grams milk thistleextract and 50 grams resveratrol per liter. The mixture is blended at50° C. for 60 minutes. 500 grams of glucosamine sulfate per litersolvent is added and continued mixing at 40° C. for thirty minutes.Vacuum is applied to reactor to remove solvent until dry. In anotherembodiment, using the methodology described above the ratio of curcuminto milk thistle extract to glucosamine sulfate is 1:1:1:3.

Example 4—Preparation of curcumin/milk thistle extract-N-acetyl-cysteinecomplex. A curcumin/milk thistle extract-N-acetyl-cysteine complex wasprepared for administration to human and animal subjects. The followingmaterials were used: N-acetyl-cysteine was 99% by weight, curcumin was95% curcuminoids by weight, milk thistle extract was 80% silymarin (and30% silibinin) by weight and 100% ethyl alcohol. Ratio of curcumin:milkthistle extract:whey protein isolate is 1:1:4 w/w. A 0.5% w/v tincture(solution) was prepared by mixing 200 g curcumin powder and 200 grammilk thistle extract powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g N-acetyl-cysteine powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and milk thistleextract are added to a 2000 ml. solvent (ethanol) at the rate of 100grams (each) per liter. The mixture is blended at 50° C. for 60 minutes.400 grams of N-acetyl-cysteine per liter solvent is added and continuedmixing at 40° C. for thirty minutes. Vacuum is applied to reactor toremove solvent until dry. In another embodiment, using the methodologydescribed above the ratio of curcumin to milk thistle extract toN-acetyl-cysteine is 1:1:2.

Example 5—Preparation of curcumin/milk thistle extract-DL-methioninecomplex. A curcumin/milk thistle extract-DL-methionine complex wasprepared for administration to human and animal subjects. The followingmaterials were used: DL-methionine was 99% by weight, curcumin was 95%curcuminoids by weight, milk thistle extract was 80% silymarin (and 30%silibinin) by weight and 100% ethyl alcohol. Ratio of curcumin:milkthistle extract:whey protein isolate is 1:1:4 w/w. A 0.5% w/v tincture(solution) was prepared by mixing 200 g curcumin powder and 200 grammilk thistle extract powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g N-acetyl-cysteine powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and milk thistleextract are added to a 2000 ml. solvent (ethanol) at the rate of 100grams (each) per liter. The mixture is blended at 50° C. for 60 minutes.400 grams of DL-methionine per liter solvent is added and continuedmixing at 40° C. for thirty minutes. Vacuum is applied to reactor toremove solvent until dry. In another embodiment, using the methodologydescribed above the ratio of curcumin to milk thistle extract toDL-methionine is 1:1:2.

Example 6—Preparation of curcumin/milk thistleextract/resveratrol-N-acetyl-cysteine complex. A curcumin/milk thistleextract/resveratrol-N-acetyl-cysteine complex was prepared foradministration to human and animal subjects. The following materialswere used: N-acetyl-cysteine was 99% by weight, curcumin was 95%curcuminoids by weight, milk thistle extract was 80% silymarin (and 30%silibinin) by weight, resveratrol as 98% by weight and 100% ethylalcohol. Ratio of curcumin:milk thistleextract:resveratrol:N-acetyl-cysteine is 2:2:1:10 w/w. A 0.5% w/vtincture (solution) was prepared by mixing 200 g curcumin powder and 200gram milk thistle extract powder and 100 grams resveratrol with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes. To the resulting solution was added 1000 g N-acetyl-cysteinepowder. The mixture was placed on a rotary evaporator (rotovap) at slowspeed (20-30 rpm), having a water bath temperature of 50° C., and lowvacuum for 3-4 hours or until the ethanol was evaporated. Alternatively,the mixture was placed in a lyophilizer. The final product was acrystalline, fine and orange colored powder. The powder re-solubilizesin water with stirring. Alternative method—In a vacuum blender thecurcumin and milk thistle extract are added to a 2000 ml. solvent(ethanol) at the rate of 100 grams of curcumin, 100 grams milk thistleextract and 50 grams resveratrol per liter. The mixture is blended at50° C. for 60 minutes. 500 grams of N-acetyl-cysteine per liter solventis added and continued mixing at 40° C. for thirty minutes. Vacuum isapplied to reactor to remove solvent until dry. In another embodiment,using the methodology described above the ratio of curcumin to milkthistle extract to N-acetyl-cysteine is 1:1:1:3.

Example 7—Preparation of curcumin/milk thistle extract-hemp proteinisolate complex. A curcumin/milk thistle extract-whey protein isolatecomplex was prepared for administration to human and animal subjects.The following materials were used: hemp protein isolate was 70% proteinby weight, curcumin was 95% curcuminoids by weight, milk thistle extractwas 80% silymarin (and 30% silibinin) by weight and 100% ethyl alcohol.Ratio of curcumin:milk thistle extract:hemp protein isolate is 1:1:100w/w. A 0.5% w/v tincture (solution) was prepared by mixing 10 gramscurcumin powder and 10 grams milk thistle extract powder with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes or until solution turned clear. To the resulting solution wasadded 1000 g hemp protein isolate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product is a fine and yellow tan colored powder.The powder re-solubilizes in water with stirring. Alternative method—Ina vacuum blender the curcumin and milk thistle extract are added to a2000 ml. solvent (ethanol) at the rate of 5 grams (each) per liter. Themixture is blended at 50° C. for 60 minutes or until mixture is clear.500 grams of hemp protein isolate per liter solvent is added andcontinued mixing at 40° C. for thirty minutes. Vacuum is applied toreactor to remove solvent until dry.

Example 7a—In another instance, more than one polyphenol may becomplexed with a protein, peptide, amino acid, polysaccharide,disaccharide, or monosaccharide using the same methods described above.In some embodiments, the first polyphenol is a curcuminoid and thesecond polyphenol is a milk thistle extract (80% silymarin, 30%silibinin). The protein is brown rice protein isolate. Example7b—Preparation of curcumin/milk thistle extract-brown rice proteinisolate complex. A curcumin/milk thistle extract-brown rice proteinisolate complex was prepared for administration to human and animalsubjects. The following materials were used: brown rice protein isolatewas 90% protein by weight, curcumin was 95% curcuminoids by weight, milkthistle extract was 80% silymarin (and 30% silibinin) by weight and 100%ethyl alcohol. Ratio of curcumin:milk thistle extract:brown rice proteinisolate is 1:1:40 w/w. A 0.5% w/v tincture (solution) was prepared bymixing 25 g curcumin powder and 25 gram milk thistle extract powder with2000 mL ethanol. The mixture was placed on a magnetic stirring hotplate, with a speed setting at medium, and temperature setting at 50° C.for 30 minutes or until solution turned clear. To the resulting solutionwas added 1000 g brown rice protein isolate powder. The mixture wasplaced on a rotary evaporator (rotovap) at slow speed (20-30 rpm),having a water bath temperature of 50° C., and low vacuum for 3-4 hoursor until the ethanol was evaporated. Alternatively, the mixture wasplaced in a lyophilizer. The final product was a fine and dull yellowcolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and milk thistleextract are added to a 2000 ml. solvent (ethanol) at the rate of 12.5grams (each) per liter. The mixture is blended at 50° C. for 60 minutesor until mixture is clear. 500 grams of brown rice protein per litersolvent is added and continued mixing at 40° C. for thirty minutes.Vacuum is applied to reactor to remove solvent until dry.

Example 8—Preparation of curcumin/resveratrol-whey protein isolatecomplex. A curcumin/resveratrol extract-whey protein isolate complex wasprepared for administration to human and animal subjects. The followingmaterials were used: whey protein isolate was 90% protein by weight,curcumin was 95% curcuminoids by weight, resveratrol was 98% by weightand 100% ethyl alcohol. Ratio of curcumin:resveratrol:whey proteinisolate is 1:1:40 w/w. A 0.5% w/v tincture (solution) was prepared bymixing 25 g curcumin powder and 25 gram resveratrol powder with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes or until solution turned clear. To the resulting solution wasadded 1000 g whey protein isolate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a fine and yellow colored powder. Thepowder re-solubilizes in water with stirring. Alternative method—In avacuum blender the curcumin and resveratrol are added to a 2000 ml.solvent (ethanol) at the rate of 12.5 grams (each) per liter. Themixture is blended at 50° C. for 60 minutes or until mixture is clear.500 grams of whey protein per liter solvent is added and continuedmixing at 40° C. for thirty minutes. Vacuum is applied to reactor toremove solvent until dry.

Example 9—In another instance, more than one polyphenol may be complexedwith a protein, peptide, amino acid, polysaccharide, disaccharide, ormonosaccharide using the same methods described above. In someembodiments, the first polyphenol is a curcuminoid and the secondpolyphenol is a resveratrol. The protein is brown rice protein isolate.Example 1—Preparation of curcumin/resveratrol-brown rice protein isolatecomplex. A curcumin/resveratrol-brown rice protein isolate complex wasprepared for administration to human and animal subjects. The followingmaterials were used: brown rice protein isolate was 90% protein byweight, curcumin was 95% curcuminoids by weight, resveratrol by weightand 100% ethyl alcohol. Ratio of curcumin:resveratrol:brown rice proteinisolate is 1:1:40 w/w. A 0.5% w/v tincture (solution) was prepared bymixing 25 g curcumin powder and 25 gram resveratrol powder with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes or until solution turned clear. To the resulting solution wasadded 1000 g brown rice protein isolate powder. The mixture was placedon a rotary evaporator (rotovap) at slow speed (20-30 rpm), having awater bath temperature of 50° C., and low vacuum for 3-4 hours or untilthe ethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a fine and dull yellow coloredpowder. The powder re-solubilizes in water with stirring. Alternativemethod—In a vacuum blender the curcumin and resveratrol are added to a2000 ml. solvent (ethanol) at the rate of 12.5 grams (each) per liter.The mixture is blended at 50° C. for 60 minutes or until mixture isclear. 500 grams of brown rice protein per liter solvent is added andcontinued mixing at 40° C. for thirty minutes. Vacuum is applied toreactor to remove solvent until dry.

Example 10—Preparation of curcumin/resveratrol-N-acetyl-cysteinecomplex. A curcumin/resveratrol-N-acetyl-cysteine complex was preparedfor administration to human and animal subjects. The following materialswere used: N-acetyl-cysteine was 99% by weight, curcumin was 95%curcuminoids by weight, resveratrol by weight and 100% ethyl alcohol.Ratio of curcumin:resveratrol:whey protein isolate is 1:1:4 w/w. A 0.5%w/v tincture (solution) was prepared by mixing 200 g curcumin powder and200 gram resveratrol powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g N-acetyl-cysteine powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until 90% ofthe ethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and resveratrol areadded to a 2000 ml. solvent (ethanol) at the rate of 100 grams (each)per liter. The mixture is blended at 50° C. for 60 minutes. 400 grams ofN-acetyl-cysteine per liter solvent is added and continued mixing at 40°C. for thirty minutes. Vacuum is applied to reactor to remove solventuntil dry. In another embodiment, using the methodology described abovethe ratio of curcumin to resveratrol to N-acetyl-cysteine is 1:1:2.

Example 11—Preparation of curcumin/resveratrol-glucosamine sulfatecomplex. A curcumin/resveratrol-glucosamine sulfate complex was preparedfor administration to human and animal subjects. The following materialswere used: glucosamine sulfate was 99% by weight, curcumin was 95%curcuminoids by weight, resveratrol by weight and 100% ethyl alcohol.Ratio of curcumin:resveratrol:glucosamine sulfate is 1:1:4 w/w. A 0.5%w/v tincture (solution) was prepared by mixing 200 g curcumin powder and200 gram resveratrol powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g glucosamine sulfate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and resveratrol areadded to a 2000 ml. solvent (ethanol) at the rate of 100 grams (each)per liter. The mixture is blended at 50° C. for 60 minutes. 400 grams ofglucosamine sulfate per liter solvent is added and continued mixing at40° C. for thirty minutes. Vacuum is applied to reactor to removesolvent until dry. In another embodiment, using the methodologydescribed above the ratio of curcumin to resveratrol to glucosaminesulfate is 1:1:2.

Example 12—Preparation of curcumin/milk thistle extract-chondroitinsulfate complex. A curcumin/milk thistle extract-chondroitin sulfatecomplex was prepared for administration to human and animal subjects.The following materials were used: chondroitin sulfate was 99% byweight, curcumin was 95% curcuminoids by weight, milk thistle extractwas 80% silymarin (and 30% silibinin) by weight and 100% ethyl alcohol.Ratio of curcumin:milk thistle extract:chondroitin sulfate is 1:1:4 w/w.A 0.5% w/v tincture (solution) was prepared by mixing 200 g curcuminpowder and 200 gram milk thistle extract powder with 2000 mL ethanol.The mixture was placed on a magnetic stirring hot plate, with a speedsetting at medium, and temperature setting at 50° C. for 30 minutes. Tothe resulting solution was added 800 g chondroitin sulfate powder. Themixture was placed on a rotary evaporator (rotovap) at slow speed (20-30rpm), having a water bath temperature of 50° C., and low vacuum for 3-4hours or until the ethanol was evaporated. Alternatively, the mixturewas placed in a lyophilizer. The final product was a crystalline, fineand orange colored powder. The powder re-solubilizes in water withstirring. Alternative method—In a vacuum blender the curcumin and milkthistle extract are added to a 2000 ml. solvent (ethanol) at the rate of100 grams (each) per liter. The mixture is blended at 50° C. for 60minutes. 400 grams of chondroitin sulfate per liter solvent is added andcontinued mixing at 40° C. for thirty minutes. Vacuum is applied toreactor to remove solvent until dry. In another embodiment, using themethodology described above the ratio of curcumin to milk thistleextract to chondroitin sulfate is 1:1:2.

Example 13—Preparation of curcumin/resveratrol-chondroitin sulfatecomplex. A curcumin/resveratrol-chondroitin sulfate complex was preparedfor administration to human and animal subjects. The following materialswere used: chondroitin sulfate was 99% by weight, curcumin was 95%curcuminoids by weight, resveratrol by weight and 100% ethyl alcohol.Ratio of curcumin:resveratrol:chondroitin sulfate is 1:1:4 w/w. A 0.5%w/v tincture (solution) was prepared by mixing 200 g curcumin powder and200 gram resveratrol powder with 2000 mL ethanol. The mixture was placedon a magnetic stirring hot plate, with a speed setting at medium, andtemperature setting at 50° C. for 30 minutes. To the resulting solutionwas added 800 g chondroitin sulfate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a crystalline, fine and orangecolored powder. The powder re-solubilizes in water with stirring.Alternative method—In a vacuum blender the curcumin and milk thistleextract are added to a 2000 ml. solvent (ethanol) at the rate of 100grams (each) per liter. The mixture is blended at 50° C. for 60 minutes.400 grams of chondroitin sulfate per liter solvent is added andcontinued mixing at 40° C. for thirty minutes. Vacuum is applied toreactor to remove solvent until dry. In another embodiment, using themethodology described above the ratio of curcumin to resveratrol tochondroitin sulfate is 1:1:2.

In another instance, more than one polyphenol may be complexed with aprotein, peptide, amino acid, polysaccharide, disaccharide, ormonosaccharide using the same methods described above. In someembodiments, the first polyphenol is a curcuminoid and the secondpolyphenol is a milk thistle extract (80% silymarin, 30% silibinin). Theprotein is egg protein isolate.

Example 14—Preparation of curcumin/milk thistle extract-egg proteinisolate complex. A curcumin/milk thistle extract-egg protein isolatecomplex was prepared for administration to human and animal subjects.The following materials were used: egg protein isolate was 90% proteinby weight, curcumin was 95% curcuminoids by weight, milk thistle extractwas 80% silymarin (and 30% silibinin) by weight and 100% ethyl alcohol.Ratio of curcumin:milk thistle extract:egg protein isolate is 1:1:40w/w. A 0.5% w/v tincture (solution) was prepared by mixing 25 g curcuminpowder and 25 gram milk thistle extract powder with 2000 mL ethanol. Themixture was placed on a magnetic stirring hot plate, with a speedsetting at medium, and temperature setting at 50° C. for 30 minutes oruntil solution turned clear. To the resulting solution was added 1000 gegg protein isolate powder. The mixture was placed on a rotaryevaporator (rotovap) at slow speed (20-30 rpm), having a water bathtemperature of 50° C., and low vacuum for 3-4 hours or until the ethanolwas evaporated. Alternatively, the mixture was placed in a lyophilizer.The final product was a fine and yellow colored powder. The powderre-solubilizes in water with stirring. Alternative method—In a vacuumblender the curcumin and milk thistle extract are added to a 2000 ml.solvent (ethanol) at the rate of 12.5 grams (each) per liter. Themixture is blended at 50° C. for 60 minutes or until mixture is clear.500 grams of egg protein per liter solvent is added and continued mixingat 40° C. for thirty minutes. Vacuum is applied to reactor to removesolvent until dry.

Example 15—Preparation of curcumin/resveratrol-egg protein isolatecomplex. A curcumin/resveratrol extract-egg protein isolate complex wasprepared for administration to human and animal subjects. The followingmaterials were used: egg protein isolate was 90% protein by weight,curcumin was 95% curcuminoids by weight, resveratrol was 98% by weightand 100% ethyl alcohol. Ratio of curcumin:resveratrol:egg proteinisolate is 1:1:40 w/w. A 0.5% w/v tincture (solution) was prepared bymixing 25 g curcumin powder and 25 gram resveratrol powder with 2000 mLethanol. The mixture was placed on a magnetic stirring hot plate, with aspeed setting at medium, and temperature setting at 50° C. for 30minutes or until solution turned clear. To the resulting solution wasadded 1000 g egg protein isolate powder. The mixture was placed on arotary evaporator (rotovap) at slow speed (20-30 rpm), having a waterbath temperature of 50° C., and low vacuum for 3-4 hours or until theethanol was evaporated. Alternatively, the mixture was placed in alyophilizer. The final product was a fine and yellow colored powder. Thepowder re-solubilizes in water with stirring. Alternative method—In avacuum blender the curcumin and resveratrol are added to a 2000 ml.solvent (ethanol) at the rate of 12.5 grams (each) per liter. Themixture is blended at 50° C. for 60 minutes or until mixture is clear.500 grams of egg protein per liter solvent is added and continued mixingat 40° C. for thirty minutes. Vacuum is applied to reactor to removesolvent until dry.

Clinical Case Studies—Example 1: A 60 year old male was presented withlower back pain and pain from foot arthritis. The individual suffersfrom irritable bowel syndrome (IBD). Several different dosages andformulations were given.

Formulation and Dosage Effect Side effects 700 mg conjugate once a dayorally for Symptom relief from lower Transient headache; sleep one week-back pain, foot arthritis, and disturbance; 150 mg. Curcumin IBD;significant pain relief 150 mg. Milk thistle with normal work activities50 mg. resveratrol 350 mg. glucosamine sulfate 1200 mg conjugate twice aday for two Symptom relief from lower Transient headache; sleep weeks-back pain, foot arthritis, and disturbance 30 mg. Curcumin IBD; somepain relief with 30 mg. Milk thistle normal work activities 540 mg. Wheyprotein isolate 700 mg conjugate once a day for one Symptom relief fromlower Transient headache; sleep week- back pain, foot arthritis, anddisturbance; 150 mg. Curcumin IBD; significant pain relief 150 mg. Milkthistle with normal work activities 50 mg. Resveratrol 350 mgN-acetyl-cysteine

Clinical Case Studies—Example 2: A 64 year old male was presented withlymphoma and multi-focal enlarged lymph nodes. The patient wasadministered 700 mg (350 mg. glucosamine sulfate; 150 mg.curcumin; 150mg. Milk thistle; 50 resveratrol) conjugate once a day for two weeks. Hedisplayed moderate shrinking of affected lymph nodes after two weeks.Further use of material did not have any further effect. Sideeffects—none documented

Clinical Case Studies—Example 3: A 57 year old male was presented withsmall multi-focal lipomas. The patient was administered 700 mg (350 mg.glucosamine sulfate; 150 mg.curcumin; 150 mg. Milk thistle; 50resveratrol) conjugate once a day for two weeks. There was as much as50% shrinkage in the size of the lipomas. Side effects—transientheadache.

Clinical Case Studies—Example 4: A 50 year old male suffers from painassociated with pelvic arthritis from previous injury. The patient wasadministered 700 mg (350 mg. glucosamine sulfate; 150 mg.curcumin; 150mg. Milk thistle; 50 resveratrol) conjugate once a day for two weeks.There was significant pain relief after one week. The individual hasbeen able to resume normal day to day activities. Side effects—nonenoted.

Clinical Case Studies—Example 5: A 78 year old female was presented withdebilitating arthritis in both ankles. She had pain at rest, and wasambulatory primarily in a wheelchair, with minimal ability to stand orwalk with a walker. She used various NSAIDs and prescription anti-painnarcotics daily. The patient was administered 700 mg (350 mg.glucosamine sulfate; 150 mg.curcumin; 150 mg. Milk thistle; 50resveratrol) conjugate once a day for a month. She obtained symptomrelief from arthritis, which included decreased pain and increasedmobility without the use of a wheelchair or a walker. She discontinuedthe use of the narcotics. Side effects—none noted

Clinical Case Studies—Example 6: A 28 year old white female waspresented with a history of anxiety and lack of concentration. Thepatient was administered 700 mg (350 mg. glucosamine sulfate; 150 mg.curcumin; 150 mg. Milk thistle; 50 resveratrol) conjugate once a day fortwo weeks with moderate relief of symptoms of anxiety and reportedincreased ability to concentrate on normal work activities. Sideeffects—none noted

Clinical Case Studies—Example 7: 62 year old male was presented with ahistory of moderate arthritis in left shoulder. The patient wasadministered 700 mg (350 mg. glucosamine sulfate; 150 mg.curcumin; 150mg. Milk thistle; 50 resveratrol) conjugate once a day for two weekswith moderate relief of symptoms from the arthritis in the leftshoulder. He could resume normal day to day work activities. Sideeffects—transient headache.

Clinical Animal Case Studies—Example 1: A 6 year old Golden Retrieve901b spayed female was presented lameness and lethargy associated withright shoulder arthritis and hip dysplasia. The animal was given 350 mg(175 mg. glucosamine sulfate; 75 mg.curcumin; 75 mg. Milk thistle; 25resveratrol) conjugate in the feed once a day for two weeks. The dogresumed normal behavior and significant relief from pain associated withthe arthritis. Side effects—none noted.

Clinical Animal Case Studies—Example 2: A 5 year old TB mare waspresented with osteoarthritis in both hocks. It showed pain on flexionof each hock and “rough gait” at gallop. It was orally administered 10grams (4900 mg. glucosamine sulfate; 2100 mg. curcumin; 2100 mg. MilkThistle; 700 mg resveratrol) conjugate in the feed twice a day. Afterone week, the horse showed marked decrease in pain on flexion of hocksand smooth gait at gallop, along with calming and decrease anxiety.There was no adverse side effect.

Clinical Animal Case Studies—Example 3: A 2 year old mix breed 301bspayed female displayed exercise induced lumbar vertebral trauma withmoderate pain and lethargy. The dog was administered 175 mg. (90 mgchondroitin sulfate; 36 mg curcumin; 36 mg milk thistle; 13 mgresveratrol) conjugate orally once a day for one month. The dog resumednormal activities without any signs of associated back pain andlethargy.

The Whey-protein isolates that have been treated with curcumin((1E,6E)-1,7-bis(4hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione).The analytical procedure set out was to monitor the concentration offree curcumin and its metabolite tetrahydrocurcumin (THC)1,7-Bis(4-hydroxy-3-methoxyphenyl)-3,5-heptanedione) in plasma fromtreated rats.

Mobile Phase-THC was (60% acetonitrile, 0.2% Ammonium hydroxide inwater). To a clean glass bottle, transfer 600 mL of acetonitrile, 398 mLof USP water, and 2 mL of Ammonium hydroxide and mix well. The solutioncan be stored at room temperature for up to 1 month. Mobile Phase A was(0.1% Formic Acid in Water. To a clean, glass bottle, transfer 999 mL ofUSP purified water and 1 mL of formic acid (≥98% purity), and mix well.The solution can be stored at room temperature for up to 1 month. MobilePhase B (0.1% Formic Acid in Acetonitrile). To a clean, glass bottle,transfer 999 mL of Acetonitrile, and 1 mL of formic acid (≥98% purity),and mix well. The solution can be stored at room temperature for up to 1month. Needle Wash Solution 1 and 2, and Reconstitution Solution (60%Acetonitrile in Water). To a clean, glass bottle, transfer 400 mL of USPPurified Water, and 600 mL of Acetonitrile, and mix well. The solutioncan be stored at room temperature up to 1 month. 0.5M NaH₂PO₄ was madeby Weigh approximately 27.6 g of Sodium Phosphate Monobasic, Monohydrate(MW: 137.99). Transfer the weighed reagent to a clean glass bottle andadd 400 mL of USP Purified Water to dissolve it. Mix well. The solutionmay be stored at room temperature for up to 1 month.

Preparation of Stock Solutions: Stock solutions of Curcumin andTetrahydrocurcumin were provided by Nucro-Technics at 1500 m/mL each inacetonitrile. Stock solutions of Curcumin-d6 and Tetrahydrocurcumin-d6were provided by Nucro-Technics as 100 m/mL each in acetonitrile. Allstock solutions were stored at −80° C.±10° C. Working standard solutionswere prepared as per as shown in Table 1. Solutions were usedimmediately or stored at −80° C.±10° C.

TABLE 1 Analyte working standard solutions Solution Solution to beDiluted Vol. of to be Prepared Conc. Acetonitrile Final Name Conc.(μg/mL) Name (μg/mL) Vol. (μL) (μL) Volume (μL) WS1 125; 62.5 SSA 1500;N/A 40 420 480 SSB N/A; 1500 20 WS2 12.5; 6.25 WS1 125; 62.5 20 180 200WS3 1.25; 0.625 WS2 12.5; 6.25 20 180 200 WS4 0.5; 0.25 WS3 1.25; 0.62540 60 100

Preparation of Internal Standard Solutions. WIS was prepared by dilutingthe 100 μg/mL Cucumin-d6 and Tetrahydrocurcumin-d6 internal standardstock solutions to 1000 ng/mL Cucumin-d6 and 500 ng/mLTetrahydrocurcumin-d6 respectively in Reconstitution solution. Solutionwas used immediately or stored at −80° C.±10° C.

Preparation of Calibration standards and Quality Controls. Calibrationstandards were prepared from analyte working standard solutions asindicated in Table 2. Matrix (EDTA-treated Rat MalePlasma—Bioreclaimation IVT #RATPLEDTA2-M) was acidified using phosphoricacid to 5% (v/v). Calibration standard samples and QC samples wereprepared in parallel with test samples and were injected after samplepreparation (outlined in next section).

Sample extraction procedure. De-conjugated Rat plasma samples wereprovided by toxicology and stored at −80° C.±10° C. Plasma was thawedwith protection from ambient light at room temperature. For each testsample, Calibration Standard, and QC sample, 1004 of each was pipettedinto pre-labeled tubes. 400 μL of 0.5M NaH2PO4 was added to all tubesand tubes were vortexed adequately. 1004 of WIS was added to all tubesusing a repeater pipette.

Samples were loaded onto ISOLUTE SLE+1 mL SPE cartridges and allowed toflow through. Samples were allowed to adsorb into packing for 10minutes. Cartridges were eluted with 6 mL of MTBE into glass tubesapplied as two 3 mL aliquots. Liquid was evaporated at 40° C. undernitrogen flow. 2504 of Reconsitution Solution was added to all tubes,vortexed adequately, and transferred to autosampler vials. Samples werekept at 6° C. in autosampler prior to same-day injection onto LC-MS

Acquisition and Post-Acquisition data analysis. All ‘unknown’ sampleswere bracketed with calibration standard samples. Instrument responsewas integrated peak areas to appropriate MS internal standard compounds.Responses for each compound were tabulated and a calibration curves forCurcumin and THC were assembled using Xcalibur LCquan software.

TABLE 1 Calculations for Curcumin in test articles Response CalculatedDose Group Subgroup Time Rat Response Ratio Conc. (ng/mL) 1. CurcuminWhey A 30 min 001 104339 0.01264 31.257 Powder Mixture 002 47015 0.0067516.838 B 1 h 003 66718 0.00949 23.552 004 47446 0.00593 14.849 A 2 h 00149823 0.00673 16.808 002 52832 0.00623 15.577 B 6 h 003 8710 0.001113.042* 004 7256 0.00106 2.912* 2. Curcumin powder A 30 min 005 476050.00624 15.606 006 13255 0.00164 4.344* B 1 h 007 25822 0.00279 7.150*008 28667 0.00330 8.390* A 2 h 005 17611 0.00226 5.845* 006 377120.00488 12.261 B 6 h 007 5087 0.00071 2.068* 008 5675 0.00070 2.036**below LLQC

Results of THC Determination. Instrument responses for calibration curveand QC for THC are provided in Tables 6-7. The calibration curve whichwas fit with a quadratic model ignoring the origin. Results andcalculations for the Curcumin content of test articles are shown in theTable 8.

TABLE 2 Calculations for THC in test articles Response Calculated Conc.Dose Group Subgroup Time Rat Response Ratio (ng/mL) 1. Curcumin Whey A30 min 001 263 0.00259 2.247* Powder Mixture 002 118 0.00141 1.586* B 1h 003 101 0.00116 1.450* 004 189 0.00192 1.874* A 2 h 001 128 0.001511.645* 002 85 0.00092 1.312* B 6 h 003 NF NA NC 004 NF NA NC 2. Curcuminpowder A 30 min 005 471 0.00459 3.562* 006 82 0.00087 1.289* B 1 h 007103 0.00103 1.375* 008 126 0.00125 1.500* A 2 h 005 106 0.00120 1.472*006 136 0.00147 1.620* B 6 h 007 65 0.00071 1.194* 008 82 0.00086 1.280**below LLQC; NF-non found; NA-not applicable; NC-not calculated

The main test articles in this study consist of Whey-protein isolatesthat have been treated with a Curcuminoid complex, which is comprised ofcurcumin (70-80%), demethoxy curcumin (15%-25%) and bisdemethoxycurcumin(2.5%-6.5%). As the nature of the interaction between major component,curcumin and whey-protein isolate is unclear, the determination oforganic-extractable curcumin is desired which will provide an indirectindication for the amount of curcumin that has been adsorbed to thewhey-protein isolate.

The analytical procedure set out was to monitor the amount of curcuminthat could be extracted from the supplied whey-protein isolates by atargeted LC-MS/MS method.

Extraction Solution—Acetonitrile: Methanol: Formic Acid (80:19:1) byvolume. Stock dilution solution—80% Acetonitrile: 0.1% Formic Acid byvolume. Mobile Phase—50% Acetonitrile: 0.1% Formic Acid by volume.

Analyzed samples include: 1: Whey Protein Isolate, 2: WheyProtein/Curcumin preparation.—50 mg/g, 3: Whey Protein/Curcuminpreparation—high temperature—25 mg/g and 4: Curcumin.

Preparation of Stock Solutions. A stock solution of Curcumin wasprepared from highly purified material provided by Nucro-Technics to beused as an analytical calibration standard. The stock solutions weredissolved in DMSO at the following concentrations:

Stock Compound MW Concentration Notes Curcumin 368.38 g/mol 5 mMNucro-Technics Standard (>97%) Glyoxal-bis (2-hydroxyanil) 240.26 g/mol24 mg/mL MS internal standard Stock Solutions were stored at −80° C. ±10° C.

Spiking Solution Preparation. A spiking solution (Spiking Solution A)was prepared in stock dilution solution (80% Acetonitrile: 0.1% Formicacid). The final concentration of Spiking Solution A was as follows:Final Concentration of Curcumin in Spiking solution A 25 μM

A two-fold dilution series was prepared using Spiking Solution A withstock dilution solution to produce Spiking Solutions B through J tocover the analytical range of Curcumin.

Volume if Spiking solution Calibration Volume of Stock Dilutiontransferred to this tube and Curcumin Final Level Solution in tube (μL)mixed (μL) Concentration (μL) Spiking — 500 25 Solution A Spiking 500500 12.5 Solution B Spiking 500 500 6.25 Solution C Spiking 500 5003.125 Solution D Spiking 500 500 1.563 Solution E Spiking 500 500 0.7813Solution F Spiking 500 500 0.3906 Solution G Spiking 500 500 0.1953Solution H Spiking 500 500 0.09766 Solution I Spiking 500 500 0.04883Solution JAfter transferring, each spiking solution was mixed well.

Calibration Standards and QC Preparation. Calibration standards wereprepared from the spiking solution, the MS internal standard, and MobilePhase solution. The MS internal standard concentration was chosen basedon its response during method development. The MS internal standardstock—Glyoxal-bis (2-hydroxyanil), 24 mg/mL—was diluted 1:5,000 inMobile Phase solution for use as a 10× working stock solution.

Spiked standards were inverted by hand for 5-10 seconds. Each pool wasthen mixed by vortexing for 60 seconds. Pools were labeled and stored at−80° C.±10° C.

Curcumin Final Vol Spiking Vol of mobile Calibration Concentration ofSolution Vol of MS internal phase added Total vol. Level injectable (μM)Added (μL) standard added (μL) (μL) (μL) STD A 1 20 50 430 500 STD B 0.520 50 430 500 STD C 0.25 20 50 430 500 STD D 0.125 20 50 430 500 STD E0.0625 20 50 430 500 STD F 0.03125 20 50 430 500 STD G 0.01563 20 50 430500 STD H 0.007813 20 50 430 500 STD I 0.003906 20 50 430 500 STD J0.001953 20 50 430 500 Blank 0 0 50 450 500 Double 0 0 0 500 500 Blank

Vol of MS Curcumin Final Vol Spiking Vol of internal Volume of Total QCConcentration of Solution Matrix* standard Mobile Phase volume Levelinjectable (μM) Added (μL) added (μL) added (μL) added (μL ) (μL) QC 0.520 100 50 330 500 High (Spiking solution B) QC 0.0625 20 100 50 330 500Med (Spiking solution E) QC 0.007813 20 100 50 330 500 Low (Spikingsolution H) *The matrix used for QC samples was 100 μL of supernatantfrom untreated Whey-protein isolate.

Extraction Procedure. Test Article 1, Test Article 2, Test Article 3were accurately weighed (˜100 mg of each). Test Article 4 was accuratelyweighed (˜5 mg). Each was put into labeled 15 mL polypropylenescrew-capped tubes. Extraction solution (5 mL) was added to each tubeand vortexed vigorously for 30 seconds. Suspensions were allowed to sitin the dark at RT for 30 minutes to allow extraction and proteinprecipitation to occur. Tubes were centrifuged for 2000×g for 5 minutesat RT. Supernatant was removed (1 mL) to 1.5 mL microfuge tubes andsubjected to centrifugation at 20,000×g for 30 minutes at 6° C.Supernatant was removed and stored at −80° C. Supernatant from step 4was diluted 1:100 in duplicate for each test article into Stock Dilutionsolution. Samples for injection for test articles were prepared: 10 μL1:100 diluted supernatant from step 5+50 μL MS Internal Standard+440 μLMobile Phase (total volume: 500 4). All Sample tubes including preparedstandards and QC samples were centrifuged at 20,000×g for 5 min at 6° C.Supernatant (200 μL) was transferred into a polypropylene autosamplerplate and analyzed by LC/MS/MS (10 μL injections of each). Note: Unknowntest article samples were injected twice and different times during thesample sequence. Calibration standards were injected multiple times asbrackets around unknown samples. QC samples and blanks were injected atdifferent points during sample sequence to measure any effects ofcarry-over.

Results and Interpretation Curcumin Determination. Instrument responsesfor calibration curve and QC curve are provided in Table 9 and Table 10.The calibration curve which was fit with a quadratic model ignoring theorigin. Results and calculations for the Curcumin content of testarticles is shown in Table 11.

TABLE 9 Calibration curve data for Curcumin Back Specified ResponseCalculated Calibration Concentration Ratio (to MS Concentration % % %Level (μM) Response Int Std) (μM) Difference RSD CV A 1 17804178 4.524241.006 0.59 1.37 1.31 17477326 4.49273 0.999 −0.14 18384698 4.41069 0.98−2.05 B 0.5 9553838 2.27291 0.494 −1.21 1.19 1.16 9658406 2.30265 0.5010.12 10170571 2.25004 0.489 −2.22 C 0.25 5005950 1.1894 0.256 2.21 1.621.6 5080612 1.19111 0.256 2.36 5134669 1.15758 0.249 −0.56 D 0.1252574889 0.6069 0.129 3.47 1.06 1.05 2662834 0.61886 0.132 5.53 27240430.60897 0.13 3.83 E 0.0625 1294205 0.30379 0.064 2.72 2.05 2.02 12970760.30922 0.065 4.58 1345161 0.29697 0.063 0.38 F 0.03125 654786 0.154150.032 2.94 1.15 1.12 648177 0.15135 0.032 1.02 677686 0.15106 0.032 0.83G 0.01563 323361 0.07582 0.015 −1.23 3.07 2.93 331331 0.07686 0.016 0.19360156 0.08018 0.016 4.72 H 0.007813 168790 0.03893 0.008 −3.15 5.214.74 165401 0.03941 0.008 −1.84 162555 0.03607 0.007 −10.96 I 0.00390681955 0.01917 0.003 −14.14 1.29 1.05 81709 0.01889 0.003 −15.69 919380.02076 0.004 88.97 J 0.001953 44131 0.01024 0.001 −25.87 54 39.7 463560.01056 0.002 −22.3 45666 0.01049 0.002 −23.1

TABLE 10 QC sample data for Curcumin Back Specified Calculated QCConcentration Response Ratio Concentration % % % Level (μM) Response (toMS Int Std) (μM) Difference RSD CV High 0.5 8107909 2.34762 0.511 2.120.66 0.64 8104125 2.37389 0.516 3.29 Medium 0.0625 1037969 0.29641 0.0630.18 2.36 2.33 1077488 0.30635 0.065 3.59 Low 0.007813 145761 0.041820.008 4.75 6.61 6.04 136858 0.0384 0.007 −4.61

TABLE 11 Calculations for Curcumin in test articles Sample dilutionCalculated Curcumin Original Test % of on factor Concentration in 5 mLarticle original Response (from 5 mL (μM) in the organic Weighed forTest Test Ratio organic 5 mL organic extract Mean Std extraction ArticleArticle Replicate Injection Response (to MS Int Std) extract extract(mg) (mg) Dev (mg) by weight 1 1 1 6085* 0.0015 5000 0 0 0 — 99.9 — 29107* 0.00218 5000 0 0 2 1 5224* 0.00126 5000 0 0 2 3094* 0.00074 5000 00 2 1 1 5150104 1.24409 5000 1335 2.459 2.530 0.1021 100.5  2.5% 25181937 1.2346 5000 1325 2.441 2 1 5290790 1.2928 5000 1390 2.560 25325111 1.34102 5000 1445 2.662 3 1 1 1301617 0.32125 5000 340 0.6260.626 0.0130 100.1 0.63% 2 1243747 0.31355 5000 330 0.608 2 1 12516580.32398 5000 345 0.635 2 1310155 0.32835 5000 345 0.635 4 1 1 65540501.60788 5000 1735 3.196 3.219 0.0555 5.008  64% 2 6302833 1.61644 50001745 3.214 2 1 6430208 1.65946 5000 1790 3.297 2 6666139 1.5932 50001720 3.168 *below detection limit

Interpretation for Curcumin Determination for Test Articles. For TestItem 2, the calculated organic-extractable curcumin as percent by weightof the original test article was 2.5%. Test Item 2 was prepared ascontaining 5% by weight of Test Item 4 (a curcuminoid complex) whichbased on our analysis of the curcuminoid complex contains 64% curcumin.Thus, Test Item 2 should contain 3.2%, but only 2.5% was recovered. Thiswould suggest that 22% of the total curcumin is unaccounted for assumingthat 100% of the curcumin was extractable by our method. This fractionof curcumin that is unaccounted could be a combination of degradation ofcurcumin from formulation in the Test Item or incomplete extraction ofcurcumin from the Test Item. While incomplete extraction could be due toinsufficient organic solvent used, and would need to be investigated,this explanation is unlikely as curcumin is readily soluble in variouspolar organic solvents. Thus it may likely that curcumin has been atleast partially adsorbed (very tightly bound or covalently linked) tothe whey-protein isolate in the Test Item. Test Item 3 was calculated tohave 0.63% by weight of organic-extractable curcumin. Test Article 3 wasformulated with 2.5% by weight of Test Item 4, thus it should contain1.6% by weight of curcumin. As this formulation underwent heating duringpreparation, there is the possibilty that some curcumin was lost duringthis step. Additional reasons, for the difference between the curcuminthat should be present in Test Item 3 and what was measured would be thesame as those raised for Test Article 2. Test Article 4 was calculatedto contain 64% by weight of curcumin and is within range of the supposedconcentration (70-80%) for curcumin in curcumin complex.

Results and Interpretation for Demethoxycurcumin andBisdemethoxycurcumin. Since demethoxycurcumin and bisdemethoxycurcuminare components of the original curcuminoid complex, an attempt was madeto detect these components in Test Items 2 and 4. As they were easilydetectable in these Test items, they were optimized for fragmentation inthe mass spectrometer and were measured by MRM using LC-MS/MS similar tocurcumin. The important differences are that no calibration curve wasused for demethoxycurcumin and bisdemethoxycurcumin.

In Table 12 and Table 13, the results for bisdemethoxycurcumin anddemethoxycurcumin and are presented. There is a calculation for theratio of the ratios of response between bisdemethoxycurcumin ordemethoxycurcumin and Curcumin. This should only be considered a roughestimate of ratio between the compounds as they are not corrected usingheavy isotope-labeled internal standards for each compound. Nonetheless,the percentages calculated are close to their reported content in thecurcuminoid complex.

TABLE 12 Response for Bisdemethoxycurcumin in Test Articles Ratio ofResponse ratios Response Bis dimethoxy Ratio curcumin: Test ArticleReplicate Injection Response (to MS Int Std) Curcumin Mean 1 1 1 2286*0.00056 — 2 2208* 0.00053 — 2 1 1975* 0.00048 — 2 1285* 0.00031 — 2 1 1122931 0.0297 2.39 2.22 2 123213 0.02936 2.38 2 1 106189 0.02595 2.01 2112485 0.02833 2.11 3 1 1 58944 0.01455 4.53 4.51 2 62658 0.0158 5.04 21 54875 0.0142 4.38 2 53513 0.01341 4.08 4 1 1 287430 0.07051 4.39 4.412 283275 0.07265 4.49 2 1 275836 0.07119 4.29 2 297199 0.07103 4.46*below detection limit

TABLE 13 Response for Demethoxycurcumin in Test Articles % Ratio ofResponse ratios Response Demethoxy Mean Test Ratio curcumin: % ofArticle Replicate Injection Response (to MS Int Std) Curcumin Curcumin 11 1 1510*   0.00037 — 2 1260*   0.0003 — 2 1 1867*   0.00045 — 2 1763*  0.00042 — 2 1 1 917312 0.22159 17.81 18.05 2 930972 0.2218 17.97 2 1976266 0.23855 18.45 2 957214 0.24106 17.98 3 1 1 318279 0.07855 24.4525.42 2 322849 0.08139 25.96 2 1 319002 0.08257 25.49 2 337224 0.0845125.74 4 1 1 1774018 0.43521 27.07 27.25 2 1701003 0.43624 26.99 2 11742916 0.4498 27.11 2 1855329 0.44342 27.83 *below detection limit

Results for Pepsin digestion and mass spectrometry of Test Articles 1,2, and 3. After initial dissolution to 10 mg/mL in 0.1% formic acid, alltest articles appears to be colloidal indicating a lack of solubility atthis concentration. Centrifugation resulted in a compact pellet in eachcase along with clear supernatant. The supernatant for Test article 1was colourless while Test articles 2 and 3 had bright yellowsupernatants. A protein assay was performed on the supernatants and isshown in Table 14 and is indicative of a saturated solution in 0.1%formic acid in which each solution contained equal amounts of protein(˜1 mg, Table) for pepsin digestion and mass spectrometry.

TABLE 14 Results of Protein assay of Supernatant for Pepsin DigestionTest Mean Protein (mg/mL) in Amount of protein Article 0.1% formic acidtreated with Pepsin (mg) 1 5.968 1.194 2 5.374 1.075 3 5.656 1.131

Protein Search results. The top-ranking proteins identified (10 or moreassigned peptide spectra) in the test articles according to number ofpeptide assigned are shown in Table 15. While there are no majordifferences in the protein identifications between the test articles, itwas noted that Test Article 3 had far fewer peptides assigned to theidentified proteins. This could be due to the heat-treatment of TestArticle 3 causing protein modifications that are not accounted forduring the peptide matching, or due to a stochastic event during themass spectrometry (only one injection of each pepsin-digested testarticles was performed). Modification of any amino acid for the mass ofcurcumin and its theoretical covalently modified species (368.13,370.40, and 352.00) were added to detect potential modifications oradducts. This modification was assigned to few low scoring peptides forsome proteins identified in Test Articles 1 and 2 indicating thatassignments could be non-specific as Test Article 1 did not containcurcumin.

TABLE 15 Proteins identified in Test Articles with >10 spectra Number ofAssigned Spectra Accession Molecular Test Test Test Identified ProteinsNumber Weight Article 1 Article 2 Article 3 Major allergenbeta-lactoglobulin B5B0D4_ 20 kDa 357 447 95 OS = Bos taurus PE = 2 SV =1 BOVIN Beta-casein OS = Bos taurus GN = CSN2 CASB_ 25 kDa 128 150 37 PE= 1 SV = 2 BOVIN Glycosylation-dependent cell adhesion GLCM1_ 17 kDa 108121 42 molecule 1 OS = Bos taurus BOVIN GN = GLYCAM1 PE = 1 SV = 2 Serumalbumin OS = Bos taurus ALBU_ 69 kDa 51 42 0 GN = ALB PE = 1 SV = 4BOVIN Alpha-lactalbumin protein variant D G9G9X6_ 16 kDa 42 43 0 OS =Bos taurus GN = LALBA PE = 3 BOVIN (+1) SV = 1 Kappa-casein OS = Bostaurus CASK_ 21 kDa 0 40 0 GN = CSN3 PE = 1 SV = 1 BOVIN Alpha-S1-caseinOS = Bos taurus CASA1_ 25 kDa 43 55 0 GN = CSN1S1 PE = 1 SV = 2 BOVINAlpha-S2-casein OS = Bos taurus CASA2_ 26 kDa 36 44 0 GN = CSN1S2 PE = 1SV = 2 BOVIN Uncharacterized protein (Fragment) G3N0V0_ 36 kDa 26 25 0OS = Bos taurus PE = 1 SV = 1 BOVIN Putative uncharacterized proteinA5D7Q2_ 52 kDa 14 21 0 OS = Bos taurus PE = 2 SV = 1 BOVIN OsteopontinOS = Bos taurus GN = SPP1 OSTP_ 31 kDa 15 15 0 PE = 1 SV = 2 BOVIN (+1)Polymeric immunoglobulin receptor PIGR_ 82 kDa 0 15 0 OS = Bos taurus GN= PIGR PE = 2 BOVIN SV = 1 Alpha-1-acid glycoprotein OS = Bos A1AG_ 23kDa 14 13 0 taurus GN = ORM1 PE = 2 SV = 1 BOVIN (+1) Butyrophilinsubfamily 1 member A1 BT1A1_ 59 kDa 15 16 0 OS = Bos taurus GN = BTN1A1PE = 1 BOVIN SV = 2 Transthyretin OS = Bos taurus GN = TTR TTHY_ 16 kDa0 11 0 PE = 1 SV = 1 BOVIN

Comparison using Progenesis QI for Proteomics. As the potentialmodification of peptides with curcumin remains undefined, a comparisonbetween Test Articles 1 and 2 was made that is independent of proteinidentification and peptide assignments. For this comparison, theretention time versus the m/z pattern of each run was compared usingProgenesis QI for Proteomics (Demo licence; Non-Linear Dynamics) withthe assumption that a curcumin modification will change the retentiontime and the mass-to-charge ratio (m/z) of the peptide. An overview ofboth runs demonstrates that the majority of ‘features’—moleculesdetected by the mass spectrometer—are very similar between the samples.The software detected over 21,000 features, with over 1,700 showingabundance changes of greater than 500 fold (see report). While many ofthese changes are due to variations in the alignment between the runs,there are several that may represent peptides that are modified by thecurcumin treated. It is anticipated that the most specific changes wouldbe represented by 1) appearance of a new feature in Test Article2—representing the modified peptide, and 2) a decrease in intensity of afeature in Test Article 2 compared with Test Article 1—representing thefraction of the material that is modified as it is unlikely that themodification will occur for all peptides.

In vitro studies, Characterization of the Curcumin Whey Protein Mixture:The “free curcumin” content of the conjugate in reference to thecurcumin whey protein mixture will be determined by extracting thecurcumin whey protein mixture and raw curcumin powder into an organicsolvent and measuring the levels of curcumin using an LC-MS basedmethod. The potential for the binding of curcumin covalently to the wheyprotein will be investigated by subjecting the conjugate and wheyprotein to enzyme digestion and evaluating peptide fragments incomparison to a digested sample of the whey protein alone using an LC-MSmethod to determine the nature of the fragments and comparatively if anyof the fragments have curcumin bound to them. When complete, thesestudies will clarify the nature of the test material as to its contentof either free curcumin or covalently linked curcumin or both. Thesestudies will be critical to evaluation of the critical analytes to besearched for when conducting in vivo studies in rats which will include,curcumin, the metabolite tetrahydrocurcumin (THC), and curcumin or THCpotentially bound to either a peptide or amino acid.

This study quantified the plasma levels of curcumin and THC followingthe dose of rats with curcumin powder and a curcumin whey proteinconjugate following oral dosing at doses of 12 mg/kg and 240 mg/kg,respectively. In addition, two other components of the curcumin powder,demethoxy and bis-demethoxy curcumin were qualitatively analyzed.

Analysis of plasma levels of total curcumin and THC following the dosingof rats with curcumin powder and the curcumin whey protein complexresulted in only detectable levels (above the limit of quantification)being observed for curcumin. Curcumin was orally absorbed from bothpreparations rapidly with T_(max) values of 0.5 hr. Plasma curcuminlevels were higher following dosing with the curcumin whey proteincomplex compared to dosing with an equivalent dose of the curcuminpowder alone. The C_(max) and AUC0-∞ values were higher by 2.4-fold and2.0-fold for the curcumin whey protein complex compared to the powder,respectively. Oral clearance and volume of distribution were high andcomparatively lower (by 2.0-fold and 2.5-fold, respectively) forcurcumin derived following dosing with the whey protein complex comparedto the powder; the oral clearance values were consistent with theliterature.

The plasma peak areas for demethoxycurcumin and bis-demethoxycurcuminidentified at their masses showed a similar profile of increase anddecrease when compared to curcumin. The peak areas at each time pointwere similar between the demethoxy and bis-demethoxy following dosingwith the curcumin whey protein complex and the curcumin powdersuggesting a similar absorption of these components from the two oralpreparations. In conclusion, plasma curcumin levels were higher in ratsorally dosed with curcumin whey protein complex compared to oral dosingwith curcumin powder alone by ˜2-fold.

The objective of this study was to measure the plasma levels of totalcurcumin and its metabolite tetrahydrocurcumin (THC) following dosingwith a curcumin Whey protein conjugate and for comparison, an equivalentdose of curcumin powder in Sprague Dawley rats. Two other components ofthe curcumin powder, demethoxycurcumin and bis-demethoxycurcumin werequalitatively evaluated. Tissue distribution was to be studied only ifsubstantial plasma levels of curcuminoids were found in the plasma.

Curcumin Whey Protein Conjugate. An appropriate amount of curcumin wheyprotein conjugate was weighed and to which was added a solution of 0.5%w/v Methyl Cellulose in sterile water for injection 0.1% v/v Tween-80(v/v) such that the final concentration of the curcumin whey proteinconjugate was 24 mg/mL (and contained 1.2 mg/mL as curcumin). Themixture was vortexed and sonnicated for 10 seconds prior to being keptstirring at room temperature prior to dosing.

Curcumin Complex. An appropriate amount of curcumin complex was weighedand to which was added a solution of 0.5% w/v Methyl Cellulose insterile water for injection 0.1% v/v Tween-80 (v/v) such that the finalconcentration of the curcumin complex was 1.2 mg/mL. The mixture wasvortexed and sonnicated for 10 seconds prior to being kept stirring atroom temperature prior to dosing.

Species: Rattus norvegicus; Strain: CD® [Crl:CD®(SD)BR](Sprague-Dawley); Source: Charles River Canada Inc., Montreal, PQ; TotalNo. of Animals on Study: 8 Males; No. of Study Groups: 2; No. of Animalsper Group: 4; Body Weight: 314.0-328.3 g at start of dosing; Age: 10-13weeks at start of dosing; Acclimatization Period: 10 days.

Animal Housing, Identification and Maintenance/Environment. Male ratswere used for this study. The animals were housed individually inNalgene® rat cages, and were identified with a unique permanent marking.The animal number and group number also appeared on a color-coded cardattached to the outside of each animal's cage. The animal roomenvironment was controlled (targeted ranges: temperature 18-26° C.,relative humidity 30-70%, greater than 10 air changes/hour) andmonitored. The photo-cycle was 12 hours light and 12 hours dark. Thecage cleaning schedule, air filtration and recirculation, health checksand facility maintenance were carried out in accordance with theapplicable Nucro-Technics' Standard Operating Procedures and suchactivities were recorded in the animal room records. Diet/Water. TekladCertified Rodent Diet (#8728C) and municipal water were provided to theanimals. It is considered that there were no known contaminants in theanimals' diet or water that might have influenced the outcome of thisstudy. Animal Welfare. The testing facility complied with all localregulations governing the care and use of laboratory animals. Proceduresare designed to avoid or minimize discomfort, distress and pain to therats in accordance with the principles of the Ontario Animals ForResearch Act (RSO 1990, Chapter A.22); Guide for the Care and Use ofLaboratory Animals, 8th Edition, NRC, 2011; and the Guidelines ofCanadian Council on Animal Care (CCAC). The CCAC Guide for the Care andUse of Experimental Animals and reacted polices and the AAALAC Guide forthe Care and Use of Laboratory Animals, were regarded as the guidelinesto follow. The testing facility has a certificate of registration as aresearch facility under the Animals for Research Act issued by theOntario Ministry of Agriculture and Food and is accredited in GoodAnimal Practices® by the CCAC and AAALAC.

Dosing of Rats. Male Rats were orally dosed with the curcumin wheyprotein conjugate and the curcumin complex according to the study designin Table 16.

TABLE 16 Study Design Dose No. and Sex Dose Volume Concentration ofanimals Dose Group (mg/kg) (mL/kg) (mg/mL) per time point Curcumin Whey240 10 24 Subgroup A 2M Powder Mixture Subgroup B 2M Curcumin 12 10 1.2Subgroup A 2M Powder Subgroup B 2M M denotes male rats

Blood samples 0.6-0.8 mL were taken according to the schedule below at0.5, 1, 2 and 6 hrs postdosing as described in Table 17 into tubescontaining K2EDTA.

Organ/tissue collection was performed following the last bleed at 2 and6 hours as described in Table 18. The following organs/tissues werecollected: brain, kidneys, major lobes of the lung and liver, pancreasand one whole joint of the knee and ankle combined. The organs werehomogenized in 5 volumes per gram wet-weight of 0.5 M NaH₂PO₄, usingthree 5-second bursts of a polytron. The resulting homogenates werefrozen (at −80±10° C.) pending possible analysis.

Plasma was separated by centrifugation, the plasma isolated andmaintained in the dark at 2-8° C. Following collection of all plasmasamples, they were treated with deconjugating enzymes (glucuronidase andsulfatase) to remove conjugation of curcumin in the form of glucuronidesand sulfates. Briefly, a 120 μL aliquot of plasma was treated with 10%of the plasma volume of 50 mM sodium phosphate buffer, pH 7.4 (foroptimal enzymatic pH). Subsequently, 60 μL of an enzymatic mixcontaining 5000 Units/mL of β-glucuronidase and 100 Units/mL ofsulfatase, dissolved in 0.1 M sodium acetate, pH 5.5+0.1% BSA (w/v) wasadded to the tubes. The tubes were incubated at 37° C. for 30 minutes,to which was subsequently added 5% v/v of phosphoric acid followingwhich the samples were frozen at −80±10° C. until analyzed. Duplicatesamples were taken at each time point.

TABLE 17 Blood Sampling Schedule No. and Sex of animals per time Bloodcollection Dose Group point 0.5 hr 1 hr 2 hrs 6 hrs Curcumin WheySubgroup A √ √ Powder Mixture 2M Subgroup B √ √ 2M Curcumin PowderSubgroup A √ √ 2M Subgroup B √ √ 2M

TABLE 18 Organ Collection No. and Sex of animals Organ/Tissue CollectionDose Group per time point 2 hrs 6 hrs 1. Curcumin Whey Subgroup A 2M √Powder Mixture Subgroup B 2M √ Subgroup A 2M √ Curcumin Powder SubgroupB 2M √Rats were observed for any untoward effects of dosing with theconjugate.

Sample Analysis. Initially, plasma samples were analyzed for curcuminand THC by LC/MS-MS using methods described. In addition, a qualitativeanalysis of the two remaining curcuminoids in the curcumin complex,demethoxy- and bis-demethoxty curcumin was performed. These twocompounds were measured using an LC-MS/MS method used in study no.312730 and analyzed separately from the primary assay of curcumin andTHC. After supplying the client with a preliminary report on the plasmalevels of total curcumin, a decision was taken not to analyze the tissuesamples for free levels of curcumin and THC at this time.

Pharmacokinetic Analysis. Plasma concentration-time data for curcuminwas analyzed by the non-compartmental method to obtain thepharmacokinetic parameters using validated PHOENIX® WINNONLIN® version6.3 software (Pharsight Corp).

The main parameters were calculated: AUC0-Tlast: Area under the plasmaconcentration-time curve from time zero to the time of the lastquantifiable concentration at time Tlast, calculated using the lineartrapezoidal rule. AUC0-∞: Area under the plasma concentration curve fromtime zero extrapolated to infinity AUC0-∞ will be calculated asAUC0-Tlast+(Clast/ke). C_(max): Maximum plasma concentration. T_(max):Time of maximum concentration determined from the nominal time of bloodsampling. Kel: Elimination rate constant. This will be estimated usinglinear regression on the terminal phase of the semi-logarithmicconcentration-time curve. A minimum of three data points will be usedfor the calculation of ke. No weighting will be applied to theregression line. t½: Terminal elimination half-life calculated fromln(2)/kel. MRTobs: Mean residence time. CLoral: Oral clearance. Vzoral:Oral volume of distribution.

The individual plasma levels of total curcumin and THC are presented inTable 19 and the average plasma levels of curcumin and THC are notshown. The pharmacokinetic parameters calculated for curcumin arepresented in Table 20. The peak areas representing the masses for thedemethoxycurcumin and bis-demethoxycurcumin components of the curcuminpowder are not shown. The oral dosing of either curcumin powder orcurcumin powder whey protein complex was well tolerated by rats.Analysis of plasma levels of total curcumin and THC following the dosingof rats with curcumin powder and the curcumin whey protein complexresulted in only detectable levels (above the limit of quantification)being observed for curcumin. For the analysis of the pharmacokineticparameters of curcumin, both plasma levels above and below the limit ofquantification were employed. Curcumin was orally absorbed from bothpreparations rapidly with T_(max) values of 0.5 hr. Plasma curcuminlevels were higher following dosing with the curcumin whey proteincomplex compared to dosing with an equivalent dose of the curcuminpowder alone. The C_(max) and AUC0-∞ values were higher by 2.4-fold and2.0-fold for the curcumin whey protein complex compared to the powder,respectively. Oral clearance and volume of distribution were high andcomparatively lower (by 2.0-fold and 2.5-fold, respectively) forcurcumin derived following dosing with the whey protein complex comparedto the powder. The magnitude of the oral clearance for curcumin observedin this study is consistent with that observed previous studies, wherean oral clearance of 108.5 L/kg/hr for curcumin was observed.

Given the low levels of THC observed, a pharmacokinetic analysis was notperformed. However, the levels were quite similar following dosing withthe curcumin whey protein complex and the powder. Althoughquantification of the demethoxy and bis-demethoxy curcumin components ofthe complex was not undertaken, the plasma peak areas identified attheir masses showed a similar profile of increase and decrease whencompared to curcumin. The peak areas at each time point were slightlyless and similar for the demethoxy and bis-demethoxy, respectfully, whencomparing dosing with the curcumin whey protein complex and the curcuminpowder, suggesting more or less similar absorption of these componentsfrom the two oral preparations.

The data from this study was compared to a literature study in which twopowder forms of curcumin were orally administered to rats either ascurcumin powder alone or curcumin powder in a capsule formulation; eachform of curcumin was dosed to rats at 100 mg/kg and plasma levels oftotal curcumin (free, glucuronidated and sulfated) determined up to 2hrs post-dosing. Normalization of the AUC0-2 hr for the two dose forms(AUC in ng-hr/mL/Dose in mg/kg) resulted in values of 2.3 for curcuminpowder and 3.2 for curcumin in the capsule. In the current study, theAUC0-2 hrs for total curcumin (deconjugated) for the curcumin powder was26.31 ng-hr/mL and for the curcumin whey protein complex was 56.7ng-hr/mL. Since curcumin is ˜75% curcumin, the actual dose of curcuminwas 9 mg/kg as opposed to 12 mg/kg as the complex. Normalization of thetotal curcuminoid AUC0-2 hrs from this study to the dose of curcuminlead to values of 2.9 for the curcumin powder and 6.3 for the curcuminwhey protein complex. The dose normalized values for the AUC0-2 hrs oftotal curcuminoids for the curcumin powder are in excellent agreementwith the literature, while the value for the curcumin powder wheyprotein complex suggests that it can deliver more curcumin systemicallycompared to curcumin powder alone.

TABLE 19 Total Curcumin and THC Found in Rat Plasma Samples Curcumin THCTime Concentration Concentration Dose Group Subgroup (hr) Rat (ng/mL)(ng/mL) 1. Curcumin Whey A 0.5 001 31.257 2.247* Powder Complex 00216.838 1.586* B 1 003 23.552 1.450* 004 14.849 1.874* A 2 001 16.8081.645* 002 15.577 1.312* B 6 003 3.042* NC 004 2.912* NC 2. Curcumin A0.5 005 15.606 3.562* Powder 006 4.344* 1.289* B 1 007 7.150* 1.375* 0088.390* 1.500* A 2 005 5.845* 1.472* 006 12.261 1.620* B 6 007 2.068*1.194* 008 2.036* 1.280* *below LLQC; NC—not calculated, no peak found

TABLE 20 Pharmacokinetic Parameters for Curcumin in Rats Dosed WithCurcumin Whey Protein Complex and Curcumin Powder AUC C_(max) T_(max)AUC_(0−Tlast) AUC_(0−∞) K_(el) Extrapolation t_(1/2) MRTobs CL_(oral)Vz_(oral) Group (ng/mL) (hr) (ng-hr/mL) (ng-hr/mL) (hr⁻¹) R¹ (%) (hr)(hr) (L/kg/hr) (L/kg) Curcumin 16.8 0.5 59 71 0.307 0.99 16 2.3 3.2 128416 Whey 40.4 0.5 131 145 0.375 0.93 9 1.8 2.5 62 166

The elimination pharmacokinetic parameters for curcumin were based onregression of three plasma concentration time points between 1 and 6 hrspost dosing and past the Cmax concentration. ¹Coefficient of linearregression for determination of Kel, the terminal phase elimination rateconstant.

Acute Dosing, Pharmacokinetics and Tissue Distribution of aCurcumin-Whey Protein Conjugate. (i) Male Rats will be orally dosed withthe curcumin whey protein mixture (as a suspension in 0.5% Methocel orformulation designed by the Client) at a human total daily equivalent(60 kg human at 2.4 g/day, 40 mg/kg) rat dose of 240 mg/kg and forcomparison the equivalent of the curcumin powder (95%, Curcumin complex)used to prepare the conjugate, also suspended in 0.5% methocel accordingto the study design in Table 21.

TABLE 21 Study Design Dose No. and Sex of Dose Volume Concentrationanimals per time Dose Group (mg/kg) (mL/kg) (mg/mL) point Curcumin Whey240 10 24 Subgroup A 2M Powder Mixture Subgroup B 2M Curcumin Powder 1210 1.2 Subgroup A 2M Subgroup B 2M M denotes male rats

Blood samples 0.6-0.8 mL will be taken according to the schedule belowat 0.5, 1, 2 and 6 hrs postdosing as described in Table 22 into tubescontaining K₂EDTA.

Organ/tissue collection will be done performed following the last bleedat 2 and 6 hours as described in Table 23. The following organs/tissueswill be collected: brain, kidneys, major lobes of the lung and liver,pancreas and either the whole joint or the articular cartilage of theknee (and/or ankle or both). The organs will be homogenized in 5 volumesper gram wet-weight of 0.5 M NaH₂PO₄, using three 5-second bursts of apolytron. The resulting homogenate will be frozen (at −80±10° C.)pending analysis.

Plasma will be separated by centrifugation, the plasma isolated andmaintained in the dark at 2-8° C. Following collection of all plasmasamples, they will be treated with deconjugating enzymes (glucuronidaseand sulfatase) to remove conjugation in the forms of glucuronides andsulfates. Briefly, a 120 μL aliquot of plasma will first be treated with10% of the plasma volume of 50 mM sodium phosphate buffer, pH 7.4 (foroptimal enzymatic pH). Subsequently, 60 μL of an enzymatic mixcontaining 5000 Units/mL of β-glucuronidase and 100 Units/mL ofsulfatase, dissolved in 0.1 M sodium acetate, pH 5.5+0.1% BSA (w/v) willbe added to the tubes. The tubes will be incubated at 37° C. for 30minutes, to which will be subsequently added 5% v/v of phosphoric acidfollowing which the samples will be frozen at −80±10° C. until analyzed.Duplicate samples will be taken at each time point. Total curcumin andTHC in the plasma will be quantificated by LC-MS. Potentialnon-conjugated plasma curcumin metabolites will be identified byperforming metabolite scanning by LC-MS and reported. Quantification ofany of the metabolites will be dependent on the availability referencestandards.

TABLE 22 Blood Sampling Schedule No. and Sex of Blood collection DoseGroup animals per time point 0.5 hr 1 hr 2 hrs 6 hrs 1. Curcumin WheySubgroup A 2M √ √ Powder Mixture Subgroup B 2M √ √ Curcumin PowderSubgroup A 2M √ √ Subgroup B 2M √ √

TABLE 23 Organ Collection No. and Sex of animals Organ/Tissue CollectionDose Group per time point 2 hrs 6 hrs 1. Curcumin Whey Subgroup A 2M √Powder Mixture Subgroup B 2M √ Curcumin Powder Subgroup A 2M √ SubgroupB 2M √Rats were be observed for any untoward effects of dosing with theconjugate.

It will be understood that particular embodiments described herein areshown by way of illustration and not as limitations of the invention.The principal features of this invention can be employed in variousembodiments without departing from the scope of the invention. Thoseskilled in the art will recognize, or be able to ascertain using no morethan routine experimentation, numerous equivalents to the specificprocedures described herein. Such equivalents are considered to bewithin the scope of this invention and are covered by the claims.

As used in this specification and claim(s), the words “comprising” (andany form of comprising, such as “comprise” and “comprises”), “having”(and any form of having, such as “have” and “has”), “including” (and anyform of including, such as “includes” and “include”) or “containing”(and any form of containing, such as “contains” and “contain”) areinclusive or open-ended and do not exclude additional, unrecitedelements or method steps.

The term “or combinations thereof” as used herein refers to allpermutations and combinations of the listed items preceding the term.For example, “A, B, C, or combinations thereof” is intended to includeat least one of: A, B, C, AB, AC, BC, or ABC, and if order is importantin a particular context, also BA, CA, CB, CBA, BCA, ACB, BAC, or CAB.Continuing with this example, expressly included are combinations thatcontain repeats of one or more item or term, such as BB, AAA, AB, BBC,AAABCCCC, CBBAAA, CABABB, and so forth. The skilled artisan willunderstand that typically there is no limit on the number of items orterms in any combination, unless otherwise apparent from the context.

What is claimed is:
 1. A polyphenol complex comprising: atherapeutically effective amount of one or more polyphenols selectedfrom a turmeric extract, a curcumin, a curcuminoid, a grapeseed extract,a resveratrol, a milk thistle extract, a silymarin, a silibinin, a greentea extract, a epigallocatechin gallate and a quercetin; and one or morecomplexing agents conjugated to a therapeutically effective amount ofone or more polyphenols, wherein the one or more complexing agents areselected from proteins, peptides, amino acids, polysaccharides,disaccharides, monosaccharides, amino sugars, glycosaminoglycans, andglycol-proteins, disposed in a pharmaceutically acceptable excipient,diluent, or carrier.
 2. The composition of claim 1, wherein thetherapeutically effective amount of one or more polyphenols arenon-covalently conjugated to the complexing agent.
 3. The composition ofclaim 1, wherein the therapeutically effective amount of one or morepolyphenols comprise 2, 3, 4, 5, 6, or more polyphenols.
 4. Thecomposition of claim 1, wherein the proteins are selected from Wheyprotein isolate, Egg protein isolate, Oat protein isolate, Hemp protein,Sunflower protein isolate Pea protein isolate, soybean protein isolate,fishmeal, flaxseed and Brown rice protein isolate.
 5. The composition ofclaim 1, wherein the one or more complexing agents compriseN-acetylglucosamine, glucosamine sulfate or N-acetylgalactosamine,glucuronic acid, iduronic acid, galactose chondroitin and glucosamine,glycosaminoglycan Chondroitin sulfate or Glucosamine sulfate.
 6. Thecomposition of claim 1, wherein the one or more complexing agentscomprise Cysteine, N-Acetyl cysteine, Methionine, DL methionine, Lmethionine, or taurine.
 7. The composition of claim 1, wherein the oneor more complexing agents comprise Glutathione.
 8. The composition ofclaim 1, wherein the therapeutically effective amount of one or morepolyphenols comprise a turmeric extract and the one or more complexingagents are selected from whey protein isolate, egg protein isolate, oatprotein isolate, hemp protein, sunflower protein isolate pea proteinisolate, soybean protein isolate, fishmeal, flaxseed, brown rice proteinisolate, N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan, Cysteine, N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine, taurine,Glycose aminoglycans, mucopolysaccharides, polysaccharide, Chondroitinsulfate and Glucosamine sulfate, Glutathione, or a combination thereof.9. The composition of claim 1, wherein the therapeutically effectiveamount of one or more polyphenols comprise a curcuminoid and the one ormore complexing agents are selected from whey protein isolate, eggprotein isolate, oat protein isolate, hemp protein, sunflower proteinisolate pea protein isolate, soybean protein isolate, fishmeal,flaxseed, brown rice protein isolate, N-acetylglucosamine, glucosaminesulfate or N-acetylgalactosamine, glucuronic acid, iduronic acid,galactose chondroitin and glucosamine, glycosaminoglycan, Cysteine,N-Acetyl cysteine, Methionine, DL methionine, L methionine, Tyrosine,taurine, Glycose aminoglycans, mucopolysaccharides, polysaccharide,Chondroitin sulfate and Glucosamine sulfate, Glutathione, or acombination thereof.
 10. The composition of claim 1, wherein thetherapeutically effective amount of one or more polyphenols comprise aresveratrol and the one or more complexing agents are selected from wheyprotein isolate, egg protein isolate, oat protein isolate, hemp protein,sunflower protein isolate pea protein isolate, soybean protein isolate,fishmeal, flaxseed, brown rice protein isolate, N-acetylglucosamine,glucosamine sulfate or N-acetylgalactosamine, glucuronic acid, iduronicacid, galactose chondroitin and glucosamine, glycosaminoglycan,Cysteine, N-Acetyl cysteine, Methionine, DL methionine, L methionine,Tyrosine, taurine, Glycose aminoglycans, mucopolysaccharides,polysaccharide, Chondroitin sulfate and Glucosamine sulfate,Glutathione, or a combination thereof.
 11. The composition of claim 1,wherein the therapeutically effective amount of one or more polyphenolscomprise a silibinin and the one or more complexing agents are selectedfrom whey protein isolate, egg protein isolate, oat protein isolate,hemp protein, sunflower protein isolate pea protein isolate, soybeanprotein isolate, fishmeal, flaxseed, brown rice protein isolate,N-acetylglucosamine, glucosamine sulfate or N-acetylgalactosamine,glucuronic acid, iduronic acid, galactose chondroitin and glucosamine,glycosaminoglycan, Cysteine, N-Acetyl cysteine, Methionine, DLmethionine, L methionine, Tyrosine, taurine, Glycose aminoglycans,mucopolysaccharides, polysaccharide, Chondroitin sulfate and Glucosaminesulfate, Glutathione, or a combination thereof.
 12. The composition ofclaim 1, wherein the therapeutically effective amount of one or morepolyphenols comprise Epigallocatechin gallate and the one or morecomplexing agents are selected from whey protein isolate, egg proteinisolate, oat protein isolate, hemp protein, sunflower protein isolatepea protein isolate, soybean protein isolate, fishmeal, flaxseed, brownrice protein isolate, N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan, Cysteine, N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine, taurine,Glycose aminoglycans, mucopolysaccharides, polysaccharide, Chondroitinsulfate and Glucosamine sulfate, Glutathione, or a combination thereof.13. The composition of claim 1, wherein the therapeutically effectiveamount of one or more polyphenols comprise quercetin and the one or morecomplexing agents are selected from whey protein isolate, egg proteinisolate, oat protein isolate, hemp protein, sunflower protein isolatepea protein isolate, soybean protein isolate, fishmeal, flaxseed, brownrice protein isolate, N-acetylglucosamine, glucosamine sulfate orN-acetylgalactosamine, glucuronic acid, iduronic acid, galactosechondroitin and glucosamine, glycosaminoglycan, Cysteine, N-Acetylcysteine, Methionine, DL methionine, L methionine, Tyrosine, taurine,Glycose aminoglycans, mucopolysaccharides, polysaccharide, Chondroitinsulfate and Glucosamine sulfate, Glutathione, or a combination thereof.14. The composition of claim 1, wherein the therapeutically effectiveamount of one or more polyphenols comprise a milk thistle extract andthe one or more complexing agents are selected from whey proteinisolate, egg protein isolate, oat protein isolate, hemp protein,sunflower protein isolate pea protein isolate, soybean protein isolate,fishmeal, flaxseed, brown rice protein isolate, N-acetylglucosamine,glucosamine sulfate or N-acetylgalactosamine, glucuronic acid, iduronicacid, galactose chondroitin and glucosamine, glycosaminoglycan,Cysteine, N-Acetyl cysteine, Methionine, DL methionine, L methionine,Tyrosine, taurine, Glycose aminoglycans, mucopolysaccharides,polysaccharide, Chondroitin sulfate and Glucosamine sulfate,Glutathione, or a combination thereof.
 15. A nutraceutical compositioncomprising: a therapeutically effective amount of one or morepolyphenols selected from a turmeric extract, a curcumin, a curcuminoid,a grapeseed extract, a resveratrol, a milk thistle extract, a silymarin,a silibinin, a green tea extract, a epigallocatechin gallate and aquercetin; and one or more complexing agents conjugated to atherapeutically effective amount of one or more polyphenols, wherein theone or more complexing agents are selected from proteins, peptides,amino acids, polysaccharides, disaccharides, monosaccharides, aminosugars, glycosaminoglycans, glycol-proteins disposed in apharmaceutically acceptable excipient, diluent, or carrier.
 16. A methodof treating a subject suffering from a polyphenol-related disordercomprising the steps of: identifying a subject in need of treatment of apolyphenol-related disorder; and administering to the subject anutraceutical composition comprising a polyphenol-acid complexcomprising a therapeutically effective amount of one or more polyphenolsselected from a turmeric extract, a curcumin, a curcuminoid, a grapeseedextract, a resveratrol, a milk thistle extract, a silymarin, asilibinin, a green tea extract, a epigallocatechin gallate and aquercetin; and one or more complexing agents conjugated to atherapeutically effective amount of one or more polyphenols, wherein theone or more complexing agents are selected from proteins, peptides,amino acids, polysaccharides, disaccharides, monosaccharides, aminosugars, glycosaminoglycans, glycol-proteins disposed in apharmaceutically acceptable excipient, diluent, or carrier.